A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799231



Internal ID19182332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:86342553..86408028hg38UCSC Ensembl
Innerchr13:86994808..87060283hg19UCSC Ensembl
Innerchr13:85792809..85858284hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3865476
hg1965476
hg1865476
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892411
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=12
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799231
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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