A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25781854



Internal ID19180090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:104205529..104283377hg38UCSC Ensembl
Innerchr13:104857879..104935727hg19UCSC Ensembl
Innerchr13:103655880..103733728hg18UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3877849
hg1977849
hg1877849
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892441
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=14
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25781854
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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