A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593832



Internal ID16381241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:25555425..25576647hg38UCSC Ensembl
Innerchr4:25557047..25578269hg19UCSC Ensembl
Innerchr4:25166145..25187367hg18UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3821223
hg1921223
hg1821223
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8985n54
Supporting Variantsnssv994411, nssv1152896, nssv1152895, nssv1152894, nssv994410, nssv1152897
SamplesHGDP00023, 1780862575_A, HGDP00035, HGDP00740
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593832
Frequency
Sample Size17421
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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