A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892732



Internal ID19183552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:95782414..95801846hg38UCSC Ensembl
Outerchr15:95782414..95801846hg38UCSC Ensembl
Innerchr15:96325643..96345075hg19UCSC Ensembl
Outerchr15:96325643..96345075hg19UCSC Ensembl
Innerchr15:94126647..94146079hg18UCSC Ensembl
Outerchr15:94126647..94146079hg18UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3819433
hg1919433
hg1819433
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785092, essv25779356, essv25786133
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892732
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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