A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892676



Internal ID19183496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:39225815..39297045hg38UCSC Ensembl
Outerchr15:39225815..39297045hg38UCSC Ensembl
Innerchr15:39518016..39589246hg19UCSC Ensembl
Outerchr15:39518016..39589246hg19UCSC Ensembl
Innerchr15:37305308..37376538hg18UCSC Ensembl
Outerchr15:37305308..37376538hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3871231
hg1971231
hg1871231
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25778904
Samples
Known GenesC15orf54
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892676
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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