A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1173177



Internal ID15876082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:151366094..151432372hg38UCSC Ensembl
Innerchr1:151338570..151404848hg19UCSC Ensembl
Innerchr1:149605194..149671472hg18UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3866279
hg1966279
hg1866279
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv547851
Supporting Variants
SamplesHGDP00782
Known GenesPOGZ, PSMB4, SELENBP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1173177
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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