A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892623



Internal ID18836757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:23333216..23438636hg38UCSC Ensembl
Innerchr15:23578363..23683783hg19UCSC Ensembl
Outerchr15:23497049..23762348hg19UCSC Ensembl
Innerchr15:21129804..21235224hg18UCSC Ensembl
Outerchr15:21048490..21313441hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38105421
hg19265300
hg18264952
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788938, essv25791976
Samples
Known GenesGOLGA8S, LOC440243
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892623
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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