A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790458



Internal ID18835251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:19803308..19935063hg38UCSC Ensembl
Innerchr13:20377448..20509203hg19UCSC Ensembl
Innerchr13:19275448..19407203hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38131756
hg19131756
hg18131756
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 HumanHap 610
CommentsNumber of probes=26
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790458
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer