A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892662



Internal ID18836796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32880507..33256326hg38UCSC Ensembl
Outerchr15:32856006..33256326hg38UCSC Ensembl
Innerchr15:33172708..33548527hg19UCSC Ensembl
Outerchr15:33148207..33548527hg19UCSC Ensembl
Innerchr15:30960000..31335819hg18UCSC Ensembl
Outerchr15:30935499..31335819hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38400321
hg19400321
hg18400321
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788966, essv25789165
Samples
Known GenesFMN1, TMCO5B
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892662
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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