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dbVar

Database of genomic structural variation

nsv5632896

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: 155 SVs from 34 studies. See in: genome view

Submitted genomic138,789,841-138,789,841

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5632896	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	138,789,841	138,789,841
nsv5632896	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	138,474,586	138,474,586

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17159596	insertion	SAMN00006579	Sequencing	Sequence alignment	23,265

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17159596	Submitted genomic		NC_000007.14:g.138 789841_138789842in s175	GRCh38 (hg38)		NC_000007.14	Chr7	138,789,841	138,789,841
nssv17159596	Remapped	Perfect	NC_000007.13:g.138 474586_138474587in s175	GRCh37.p13	First Pass	NC_000007.13	Chr7	138,474,586	138,474,586

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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