A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892627



Internal ID19183447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:19829666..20007545hg38UCSC Ensembl
Outerchr15:19829666..20007545hg38UCSC Ensembl
Innerchr15:20034919..20212798hg19UCSC Ensembl
Outerchr15:20034919..20212798hg19UCSC Ensembl
Innerchr15:18294933..18472812hg18UCSC Ensembl
Outerchr15:18294933..18472812hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38177880
hg19177880
hg18177880
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797224
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892627
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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