A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893217



Internal ID19184037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43089269..43222743hg38UCSC Ensembl
Outerchr19:42988873..43290434hg38UCSC Ensembl
Innerchr19:43593421..43726895hg19UCSC Ensembl
Outerchr19:43493025..43794586hg19UCSC Ensembl
Innerchr19:48285261..48418735hg18UCSC Ensembl
Outerchr19:48184865..48486426hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38301562
hg19301562
hg18301562
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788929, essv25792209, essv25791536, essv25792945, essv25789553, essv25790805, essv25791830, essv25789324, essv25792342, essv25792765, essv25792338
Samples
Known GenesLOC284344, PSG11, PSG2, PSG4, PSG5, PSG9
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893217
Frequency
Sample Size3017
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


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