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dbVar

Database of genomic structural variation

nsv5948979

Organism: Homo sapiens

Study:nstd209 (Almarri et al. 2020)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

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

Publication(s):Almarri et al. 2020

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: 139 SVs from 38 studies. See in: genome view

Submitted genomic102,932,560-102,932,560

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5948979	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	102,932,560	102,932,560
nsv5948979	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	102,573,007	102,573,007

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17448355	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17448355	Submitted genomic		NC_000007.14:g.102 932560_102932561in s157	GRCh38 (hg38)		NC_000007.14	Chr7	102,932,560	102,932,560
nssv17448355	Remapped	Perfect	NC_000007.13:g.102 573007_102573008in s157	GRCh37.p13	First Pass	NC_000007.13	Chr7	102,573,007	102,573,007

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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