A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25781390



Internal ID19178916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:81138737..81188766hg38UCSC Ensembl
Innerchr13:81712872..81762901hg19UCSC Ensembl
Innerchr13:80610873..80660902hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3850030
hg1950030
hg1850030
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892397
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=12
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25781390
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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