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dbVar

Database of genomic structural variation

nsv5949754

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: 124 SVs from 26 studies. See in: genome view

Submitted genomic132,334,560-132,334,560

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5949754	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	132,334,560	132,334,560
nsv5949754	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	132,019,319	132,019,319

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17431527	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17431527	Submitted genomic		NC_000007.14:g.132 334560_132334561in s392	GRCh38 (hg38)		NC_000007.14	Chr7	132,334,560	132,334,560
nssv17431527	Remapped	Perfect	NC_000007.13:g.132 019319_132019320in s392	GRCh37.p13	First Pass	NC_000007.13	Chr7	132,019,319	132,019,319

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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