A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792616



Internal ID18832033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30194842..30491379hg38UCSC Ensembl
Innerchr15:30487045..30783582hg19UCSC Ensembl
Innerchr15:28274337..28570874hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38296538
hg19296538
hg18296538
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892642
Supporting Variants
Samples
Known GenesCHRFAM7A, DKFZP434L187, LOC101059918
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=78
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792616
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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