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dbVar

Database of genomic structural variation

nsv6032625

Organism: Homo sapiens

Study:nstd212 (Wu et al. 2021)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:104,295

Publication(s):Wu et al. 2021

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: 490 SVs from 56 studies. See in: genome view

Submitted genomic112,077,172-112,181,466

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6032625	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	112,077,172	112,181,466
nsv6032625	Remapped	Good	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	111,947,896	112,052,189

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17601307	duplication	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17601307	Submitted genomic		NC_000011.10:g.112 077172_112181466du p	GRCh38 (hg38)		NC_000011.10	Chr11	112,077,172	112,181,466
nssv17601307	Remapped	Good	NC_000011.9:g.1119 47896_112052189dup	GRCh37.p13	First Pass	NC_000011.9	Chr11	111,947,896	112,052,189

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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