A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892675



Internal ID19183495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:37539224..37550767hg38UCSC Ensembl
Outerchr15:37539224..37550767hg38UCSC Ensembl
Innerchr15:37831425..37842968hg19UCSC Ensembl
Outerchr15:37831425..37842968hg19UCSC Ensembl
Innerchr15:35618717..35630260hg18UCSC Ensembl
Outerchr15:35618717..35630260hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3811544
hg1911544
hg1811544
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785815
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892675
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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