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dbVar

Database of genomic structural variation

nsv5962891

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

Submitted genomic71,265,119-71,265,119

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5962891	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	71,265,119	71,265,119
nsv5962891	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	70,730,105	70,730,105

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17431580	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17431580	Submitted genomic		NC_000007.14:g.712 65119_71265120ins1 94	GRCh38 (hg38)		NC_000007.14	Chr7	71,265,119	71,265,119
nssv17431580	Remapped	Perfect	NC_000007.13:g.707 30105_70730106ins1 94	GRCh37.p13	First Pass	NC_000007.13	Chr7	70,730,105	70,730,105

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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