A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636897



Internal ID7023691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:73822972..73847599hg38UCSC Ensembl
Innerchr15:73822980..73847592hg38UCSC Ensembl
Outerchr15:73822965..73847607hg38UCSC Ensembl
chr15:74115313..74139940hg19UCSC Ensembl
Innerchr15:74115321..74139933hg19UCSC Ensembl
Outerchr15:74115306..74139948hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3824628
hg1924628
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15292638, essv15292639
SamplesHG01705, HG01516
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636897
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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