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dbVar

Database of genomic structural variation

nsv5970047

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: 164 SVs from 21 studies. See in: genome view

Submitted genomic124,444,486-124,444,486

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5970047	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	124,444,486	124,444,486
nsv5970047	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	126,133,055	126,133,055

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17351569	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17351569	Submitted genomic		NC_000010.11:g.124 444486_124444487in s173	GRCh38 (hg38)		NC_000010.11	Chr10	124,444,486	124,444,486
nssv17351569	Remapped	Perfect	NC_000010.10:g.126 133055_126133056in s173	GRCh37.p13	First Pass	NC_000010.10	Chr10	126,133,055	126,133,055

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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