A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792854



Internal ID19160061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:137923806..137983478hg38UCSC Ensembl
Innerchr6:138244943..138304615hg19UCSC Ensembl
Innerchr6:138286636..138346308hg18UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3859673
hg1959673
hg1859673
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890951
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=14
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792854
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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