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dbVar

Database of genomic structural variation

nsv5959013

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: 173 SVs from 18 studies. See in: genome view

Submitted genomic100,256,511-100,256,511

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5959013	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000008.11	Chr8	100,256,511	100,256,511
nsv5959013	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	101,268,739	101,268,739

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17439493	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17439493	Submitted genomic		NC_000008.11:g.100 256511_100256512in s177	GRCh38 (hg38)		NC_000008.11	Chr8	100,256,511	100,256,511
nssv17439493	Remapped	Perfect	NC_000008.10:g.101 268739_101268740in s177	GRCh37.p13	First Pass	NC_000008.10	Chr8	101,268,739	101,268,739

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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