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dbVar

Database of genomic structural variation

nsv5958052

Organism: Homo sapiens

Study:nstd209 (Almarri et al. 2020)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

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

Publication(s):Almarri et al. 2020

Links to Other Resources

Overlapping Genes

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: 143 SVs from 26 studies. See in: genome view

Submitted genomic33,277,775-33,277,775

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5958052	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	33,277,775	33,277,775
nsv5958052	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	33,502,842	33,502,842

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17396372	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17396372	Submitted genomic		NC_000002.12:g.332 77775_33277776ins6 4	GRCh38 (hg38)		NC_000002.12	Chr2	33,277,775	33,277,775
nssv17396372	Remapped	Perfect	NC_000002.11:g.335 02842_33502843ins6 4	GRCh37.p13	First Pass	NC_000002.11	Chr2	33,502,842	33,502,842

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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