A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1013012



Internal ID16306968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:170287780..170367322hg38UCSC Ensembl
Innerchr4:171208931..171288473hg19UCSC Ensembl
Innerchr4:171445506..171525048hg18UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg3879543
hg1979543
hg1879543
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596146
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)nssv1013012
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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