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dbVar

Database of genomic structural variation

nsv5962978

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: 106 SVs from 33 studies. See in: genome view

Submitted genomic32,531,415-32,531,415

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5962978	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	32,531,415	32,531,415
nsv5962978	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	32,571,027	32,571,027

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17442665	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17442665	Submitted genomic		NC_000007.14:g.325 31415_32531416ins5 2	GRCh38 (hg38)		NC_000007.14	Chr7	32,531,415	32,531,415
nssv17442665	Remapped	Perfect	NC_000007.13:g.325 71027_32571028ins5 2	GRCh37.p13	First Pass	NC_000007.13	Chr7	32,571,027	32,571,027

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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