A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1173792



Internal ID15527859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:20567472..20592419hg38UCSC Ensembl
Innerchr1:20893965..20918912hg19UCSC Ensembl
Innerchr1:20766552..20791499hg18UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3824948
hg1924948
hg1824948
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545734
Supporting Variants
SamplesHGDP00552
Known GenesCDA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1173792
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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