A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593831



Internal ID16381240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:25555425..25575562hg38UCSC Ensembl
Innerchr4:25557047..25577184hg19UCSC Ensembl
Innerchr4:25166145..25186282hg18UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3820138
hg1920138
hg1820138
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8985n54
Supporting Variantsnssv1152891, nssv1152892, nssv1152893
SamplesHGDP00226, HGDP00602, HGDP00011
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593831
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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