A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787803



Internal ID18826997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:19836431..20022425hg38UCSC Ensembl
Innerchr13:20410571..20596565hg19UCSC Ensembl
Innerchr13:19308571..19494565hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38185995
hg19185995
hg18185995
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892297
Supporting Variants
Samples
Known GenesZMYM2, ZMYM5
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=24
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787803
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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