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dbVar

Database of genomic structural variation

nsv5624751

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: 350 SVs from 60 studies. See in: genome view

Submitted genomic102,648,997-102,648,997

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5624751	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	102,648,997	102,648,997
nsv5624751	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	102,289,444	102,289,444

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17142210	insertion	SAMN00006580	Sequencing	Sequence alignment	9,409

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17142210	Submitted genomic		NC_000007.14:g.102 648997_102648998in s87	GRCh38 (hg38)		NC_000007.14	Chr7	102,648,997	102,648,997
nssv17142210	Remapped	Perfect	NC_000007.13:g.102 289444_102289445in s87	GRCh37.p13	First Pass	NC_000007.13	Chr7	102,289,444	102,289,444

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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