A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891832



Internal ID19186228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:64647102..65058252hg38UCSC Ensembl
Outerchr10:64320597..65091394hg38UCSC Ensembl
Innerchr10:66406859..66818010hg19UCSC Ensembl
Outerchr10:66080357..66851152hg19UCSC Ensembl
Innerchr10:66076865..66488016hg18UCSC Ensembl
Outerchr10:65750363..66521158hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38770798
hg19770796
hg18770796
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788134, essv25790696, essv25790373, essv25787956, essv25788188, essv25788183, essv25789838, essv25790556, essv25791156, essv25790208
Samples
Known GenesANXA2P3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891832
Frequency
Sample Size3017
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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