A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788020



Internal ID18833008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:119615669..119657099hg38UCSC Ensembl
Innerchr10:121375181..121416611hg19UCSC Ensembl
Innerchr10:121365171..121406601hg18UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg3841431
hg1941431
hg1841431
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=11
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788020
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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