A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv920079



Internal ID15867349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:132915145..132916517hg38UCSC Ensembl
Innerchr2:133672718..133674090hg19UCSC Ensembl
Innerchr2:133389188..133390560hg18UCSC Ensembl
Cytoband2q21.2
Allele length
AssemblyAllele length
hg381373
hg191373
hg181373
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv583161
Supporting Variants
Samples
Known GenesMIR7853, NCKAP5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv920079
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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