A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv996676



Internal ID16290632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:42695536..42706248hg38UCSC Ensembl
Innerchr4:42697553..42708265hg19UCSC Ensembl
Innerchr4:42392310..42403022hg18UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3810713
hg1910713
hg1810713
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv594056
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)nssv996676
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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