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dbVar

Database of genomic structural variation

nsv5958985

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 28 studies. See in: genome view

Submitted genomic96,805,012-96,805,012

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5958985	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000005.10	Chr5	96,805,012	96,805,012
nsv5958985	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000005.9	Chr5	96,140,715	96,140,715

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17423258	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17423258	Submitted genomic		NC_000005.10:g.968 05012_96805013ins3 19	GRCh38 (hg38)		NC_000005.10	Chr5	96,805,012	96,805,012
nssv17423258	Remapped	Perfect	NC_000005.9:g.9614 0715_96140716ins31 9	GRCh37.p13	First Pass	NC_000005.9	Chr5	96,140,715	96,140,715

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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