A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796833



Internal ID19178566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:101554523..101649303hg38UCSC Ensembl
Innerchr13:102206874..102301653hg19UCSC Ensembl
Innerchr13:101004875..101099654hg18UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3894781
hg1994780
hg1894780
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892438
Supporting Variants
Samples
Known GenesITGBL1
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=27
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796833
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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