A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv995206



Internal ID16289162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:34157314..34286927hg38UCSC Ensembl
Innerchr4:34158936..34288549hg19UCSC Ensembl
Innerchr4:33835331..33964944hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38129614
hg19129614
hg18129614
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593911
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)nssv995206
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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