A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581745



Internal ID16369154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:46433306..46466824hg38UCSC Ensembl
Innerchr2:46660445..46693963hg19UCSC Ensembl
Innerchr2:46513949..46547467hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3833519
hg1933519
hg1833519
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv908100
Samples
Known GenesLOC101805491
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581745
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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