A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788130



Internal ID18830990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:119615669..119652348hg38UCSC Ensembl
Innerchr10:121375181..121411860hg19UCSC Ensembl
Innerchr10:121365171..121401850hg18UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg3836680
hg1936680
hg1836680
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891891
Supporting Variants
Samples
Known GenesBAG3
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=10
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788130
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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