A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25800944



Internal ID19173846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85161123..85185603hg38UCSC Ensembl
Innerchr15:85704354..85728834hg19UCSC Ensembl
Innerchr15:83505358..83529838hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3824481
hg1924481
hg1824481
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892719
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=8
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25800944
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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