A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25789734



Internal ID19159952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:82521896..82612931hg38UCSC Ensembl
Innerchr13:83096031..83187066hg19UCSC Ensembl
Innerchr13:81994032..82085067hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3891036
hg1991036
hg1891036
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892401
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=18
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25789734
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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