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dbVar

Database of genomic structural variation

nsv5628583

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: 335 SVs from 46 studies. See in: genome view

Submitted genomic1,496,275-1,496,275

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5628583	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	1,496,275	1,496,275
nsv5628583	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	1,535,911	1,535,911

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17154833	insertion	HG03486	Sequencing	Sequence alignment	4,355

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17154833	Submitted genomic		NC_000007.14:g.149 6275_1496276ins62	GRCh38 (hg38)		NC_000007.14	Chr7	1,496,275	1,496,275
nssv17154833	Remapped	Perfect	NC_000007.13:g.153 5911_1535912ins62	GRCh37.p13	First Pass	NC_000007.13	Chr7	1,535,911	1,535,911

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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