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dbVar

Database of genomic structural variation

nsv5979127

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

Submitted genomic112,213,885-112,213,885

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5979127	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	112,213,885	112,213,885
nsv5979127	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	112,084,608	112,084,608

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17362518	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17362518	Submitted genomic		NC_000011.10:g.112 213885_112213886in s522	GRCh38 (hg38)		NC_000011.10	Chr11	112,213,885	112,213,885
nssv17362518	Remapped	Perfect	NC_000011.9:g.1120 84608_112084609ins 522	GRCh37.p13	First Pass	NC_000011.9	Chr11	112,084,608	112,084,608

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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