A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11034n54



Internal ID22778929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:164693974..164808840hg38UCSC Ensembl
chr6:165115007..165222329hg19UCSC Ensembl
chr6:165034997..165142319hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38114867
hg19107323
hg18107323
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv605238, nsv605235, nsv605237, nsv605239
SamplesHGDP00878, HGDP00872, HGDP00702, HGDP00792, HGDP00125
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11034n54
Frequency
Sample Size17421
Observed Gain18
Observed Loss0
Observed Complex0
Frequencyn/a


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