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dbVar

Database of genomic structural variation

nsv5641416

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: 109 SVs from 29 studies. See in: genome view

Submitted genomic96,083,440-96,083,440

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5641416	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	96,083,440	96,083,440
nsv5641416	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	95,712,752	95,712,752

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17144592	insertion	HG03125	Sequencing	Sequence alignment	5,031

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17144592	Submitted genomic		NC_000007.14:g.960 83440_96083441ins3 26	GRCh38 (hg38)		NC_000007.14	Chr7	96,083,440	96,083,440
nssv17144592	Remapped	Perfect	NC_000007.13:g.957 12752_95712753ins3 26	GRCh37.p13	First Pass	NC_000007.13	Chr7	95,712,752	95,712,752

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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