A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787770



Internal ID18824560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:19837561..19950565hg38UCSC Ensembl
Innerchr13:20411701..20524705hg19UCSC Ensembl
Innerchr13:19309701..19422705hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38113005
hg19113005
hg18113005
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892297
Supporting Variants
Samples
Known GenesZMYM5
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=18
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787770
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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