A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv987707



Internal ID15934977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:1532249..1617803hg38UCSC Ensembl
Innerchr4:1533976..1619530hg19UCSC Ensembl
Innerchr4:1504781..1589489hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3885555
hg1985555
hg1884709
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593317
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)nssv987707
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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