A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25783227



Internal ID18813518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:34080781..34227911hg38UCSC Ensembl
Innerchr13:34654918..34802048hg19UCSC Ensembl
Innerchr13:33552918..33700048hg18UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg38147131
hg19147131
hg18147131
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892327
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=49
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25783227
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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