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dbVar

Database of genomic structural variation

nsv5957406

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: 379 SVs from 42 studies. See in: genome view

Submitted genomic158,729,729-158,729,729

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5957406	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	158,729,729	158,729,729
nsv5957406	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	158,522,420	158,522,420

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17441713	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17441713	Submitted genomic		NC_000007.14:g.158 729729_158729730in s81	GRCh38 (hg38)		NC_000007.14	Chr7	158,729,729	158,729,729
nssv17441713	Remapped	Perfect	NC_000007.13:g.158 522420_158522421in s81	GRCh37.p13	First Pass	NC_000007.13	Chr7	158,522,420	158,522,420

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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