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dbVar

Database of genomic structural variation

nsv5979955

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: 180 SVs from 24 studies. See in: genome view

Submitted genomic124,788,710-124,788,710

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5979955	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	124,788,710	124,788,710
nsv5979955	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	126,477,279	126,477,279

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17359085	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17359085	Submitted genomic		NC_000010.11:g.124 788710_124788711in s230	GRCh38 (hg38)		NC_000010.11	Chr10	124,788,710	124,788,710
nssv17359085	Remapped	Perfect	NC_000010.10:g.126 477279_126477280in s230	GRCh37.p13	First Pass	NC_000010.10	Chr10	126,477,279	126,477,279

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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