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dbVar

Database of genomic structural variation

nsv5972660

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: 122 SVs from 23 studies. See in: genome view

Submitted genomic94,426,429-94,426,429

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5972660	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	94,426,429	94,426,429
nsv5972660	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	94,159,595	94,159,595

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17357467	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17357467	Submitted genomic		NC_000011.10:g.944 26429_94426430ins7 8	GRCh38 (hg38)		NC_000011.10	Chr11	94,426,429	94,426,429
nssv17357467	Remapped	Perfect	NC_000011.9:g.9415 9595_94159596ins78	GRCh37.p13	First Pass	NC_000011.9	Chr11	94,159,595	94,159,595

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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