A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605237



Internal ID16392646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:164709839..164795109hg38UCSC Ensembl
Innerchr6:165130872..165208598hg19UCSC Ensembl
Innerchr6:165050862..165128588hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3885271
hg1977727
hg1877727
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11034n54
Supporting Variantsnssv1154701, nssv1075786, nssv1075788, nssv1154703, nssv1154702, nssv1075787
SamplesHGDP00702, HGDP00792, HGDP00125
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605237
Frequency
Sample Size17421
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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