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dbVar

Database of genomic structural variation

nsv5659829

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

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

Publication(s):Ebert et al. 2021

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: 208 SVs from 36 studies. See in: genome view

Submitted genomic82,260,658-82,260,658

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5659829	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000017.11	Chr17	82,260,658	82,260,658
nsv5659829	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000017.10	Chr17	80,218,534	80,218,534

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17082373	insertion	HG02587	Sequencing	Sequence alignment	2,330

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17082373	Submitted genomic		NC_000017.11:g.822 60658_82260659ins2 86	GRCh38 (hg38)		NC_000017.11	Chr17	82,260,658	82,260,658
nssv17082373	Remapped	Perfect	NC_000017.10:g.802 18534_80218535ins2 86	GRCh37.p13	First Pass	NC_000017.10	Chr17	80,218,534	80,218,534

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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