A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788503



Internal ID18831281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:164206561..164851799hg38UCSC Ensembl
Innerchr6:164627593..165265288hg19UCSC Ensembl
Innerchr6:164547583..165185278hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38645239
hg19637696
hg18637696
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890994
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=129
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788503
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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