A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25789160



Internal ID19177035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:104074640..104274628hg38UCSC Ensembl
Innerchr6:104522515..104722503hg19UCSC Ensembl
Innerchr6:104629208..104829196hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38199989
hg19199989
hg18199989
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890927
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=35
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25789160
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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