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dbVar

Database of genomic structural variation

nsv5960726

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: 206 SVs from 31 studies. See in: genome view

Submitted genomic86,925,694-86,925,694

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5960726	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	86,925,694	86,925,694
nsv5960726	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	88,685,451	88,685,451

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17358346	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17358346	Submitted genomic		NC_000010.11:g.869 25694_86925695ins2 13	GRCh38 (hg38)		NC_000010.11	Chr10	86,925,694	86,925,694
nssv17358346	Remapped	Perfect	NC_000010.10:g.886 85451_88685452ins2 13	GRCh37.p13	First Pass	NC_000010.10	Chr10	88,685,451	88,685,451

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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