A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584031



Internal ID16371440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:186500151..186575956hg38UCSC Ensembl
Innerchr2:187364878..187440683hg19UCSC Ensembl
Innerchr2:187073123..187148928hg18UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg3875806
hg1975806
hg1875806
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151340
SamplesHGDP00737
Known GenesZC3H15
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584031
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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