A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv583687



Internal ID16371096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:176839593..176855947hg38UCSC Ensembl
Innerchr2:177704321..177720675hg19UCSC Ensembl
Innerchr2:177412567..177428921hg18UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3816355
hg1916355
hg1816355
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151118
SamplesHGDP01218
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv583687
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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