A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788966



Internal ID18827163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32880507..33256326hg38UCSC Ensembl
Innerchr15:33172708..33548527hg19UCSC Ensembl
Innerchr15:30960000..31335819hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38375820
hg19375820
hg18375820
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892662
Supporting Variants
Samples
Known GenesFMN1, TMCO5B
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=160
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788966
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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