A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792227



Internal ID19162697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18450119..18503037hg38UCSC Ensembl
Innerchr13:19024259..19077177hg19UCSC Ensembl
Innerchr13:17922259..17975177hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg3852919
hg1952919
hg1852919
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892288
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=21
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792227
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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