A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593640



Internal ID16381049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:8532556..8553167hg38UCSC Ensembl
Innerchr4:8534283..8554894hg19UCSC Ensembl
Innerchr4:8585183..8605794hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3820612
hg1920612
hg1820612
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152628
SamplesHGDP00776
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593640
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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