A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv907432



Internal ID16201388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:42047532..42048586hg38UCSC Ensembl
Innerchr2:42274672..42275726hg19UCSC Ensembl
Innerchr2:42128176..42129230hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg381055
hg191055
hg181055
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581617
Supporting Variants
Samples
Known GenesPKDCC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv907432
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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