A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892720



Internal ID19183540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85894859..85979545hg38UCSC Ensembl
Outerchr15:85894859..85979545hg38UCSC Ensembl
Innerchr15:86438090..86522776hg19UCSC Ensembl
Outerchr15:86438090..86522776hg19UCSC Ensembl
Innerchr15:84239094..84323780hg18UCSC Ensembl
Outerchr15:84239094..84323780hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3884687
hg1984687
hg1884687
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780040
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892720
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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