A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790048



Internal ID19182959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:38145652..38202551hg38UCSC Ensembl
Innerchr11:38167202..38224101hg19UCSC Ensembl
Innerchr11:38123778..38180677hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3856900
hg1956900
hg1856900
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891967
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=11
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790048
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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