A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15292639



Internal ID1837552
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636897
Supporting Variants
SamplesHG01705
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15292639
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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