A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582772



Internal ID16370181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:118123492..118124504hg38UCSC Ensembl
Innerchr2:118881068..118882080hg19UCSC Ensembl
Innerchr2:118597538..118598550hg18UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg381013
hg191013
hg181013
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7022n54
Supporting Variantsnssv916370
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582772
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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