A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1032704



Internal ID15539204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:134099223..134230401hg38UCSC Ensembl
Innerchr5:133434914..133566092hg19UCSC Ensembl
Innerchr5:133462813..133593991hg18UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg38131179
hg19131179
hg18131179
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv599732
Supporting Variants
Samples
Known GenesMIR3661, PPP2CA, SKP1, TCF7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1032704
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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