A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582886



Internal ID16370295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:125596165..125612669hg38UCSC Ensembl
Innerchr2:126353742..126370246hg19UCSC Ensembl
Innerchr2:126070212..126086716hg18UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg3816505
hg1916505
hg1816505
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv916676
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582886
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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