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dbVar

Database of genomic structural variation

nsv5973665

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: 66 SVs from 22 studies. See in: genome view

Submitted genomic61,861,353-61,861,353

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5973665	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	61,861,353	61,861,353
nsv5973665	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	61,628,825	61,628,825

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17349798	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17349798	Submitted genomic		NC_000011.10:g.618 61353_61861354ins2 65	GRCh38 (hg38)		NC_000011.10	Chr11	61,861,353	61,861,353
nssv17349798	Remapped	Perfect	NC_000011.9:g.6162 8825_61628826ins26 5	GRCh37.p13	First Pass	NC_000011.9	Chr11	61,628,825	61,628,825

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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