A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1027492



Internal ID16321448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:22733638..22849375hg38UCSC Ensembl
Innerchr5:22733747..22849484hg19UCSC Ensembl
Innerchr5:22769504..22885241hg18UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38115738
hg19115738
hg18115738
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597536
Supporting Variants
Samples
Known GenesCDH12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1027492
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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