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dbVar

Database of genomic structural variation

nsv393922

Organism: Homo sapiens

Study:nstd6 (Mills et al. 2006)
Variant Type:insertion
Method Type:Sequencing
Submitted on:NCBI35 (hg17)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1

Publication(s):Mills et al. 2006

Links to Other Resources

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 259 SVs from 26 studies. See in: genome view

Remapped(Score: Perfect):19,939,266-19,939,266

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv393922	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000008.11	Chr8	19,939,266	19,939,266
nsv393922	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	19,796,777	19,796,777
nsv393922	Submitted genomic		NCBI35 (hg17)	Primary Assembly		NC_000008.9	Chr8	19,841,057	19,841,057

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv412500	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv412500	Remapped	Perfect	NC_000008.11:g.199 39266_19939267insC C	GRCh38.p12	First Pass	NC_000008.11	Chr8	19,939,266	19,939,266
nssv412500	Remapped	Perfect	NC_000008.10:g.197 96777_19796778insC C	GRCh37.p13	First Pass	NC_000008.10	Chr8	19,796,777	19,796,777
nssv412500	Submitted genomic		NC_000008.9:g.1984 1057_19841058insCC	NCBI35 (hg17)		NC_000008.9	Chr8	19,841,057	19,841,057

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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