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dbVar

Database of genomic structural variation

nsv5966767

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: 80 SVs from 17 studies. See in: genome view

Submitted genomic60,927,991-60,927,991

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5966767	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	60,927,991	60,927,991
nsv5966767	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	62,687,749	62,687,749

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17362411	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17362411	Submitted genomic		NC_000010.11:g.609 27991_60927992ins4 44	GRCh38 (hg38)		NC_000010.11	Chr10	60,927,991	60,927,991
nssv17362411	Remapped	Perfect	NC_000010.10:g.626 87749_62687750ins4 44	GRCh37.p13	First Pass	NC_000010.10	Chr10	62,687,749	62,687,749

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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