A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1017040



Internal ID16310996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:178238308..178405237hg38UCSC Ensembl
Innerchr4:179159462..179326391hg19UCSC Ensembl
Innerchr4:179396456..179563385hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38166930
hg19166930
hg18166930
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596273
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1017040
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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