A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636853



Internal ID7023647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71322718..71347110hg38UCSC Ensembl
Innerchr15:71323218..71346610hg38UCSC Ensembl
Outerchr15:71321718..71348110hg38UCSC Ensembl
chr15:71615057..71639449hg19UCSC Ensembl
Innerchr15:71615557..71638949hg19UCSC Ensembl
Outerchr15:71614057..71640449hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3824393
hg1924393
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15285193, essv15285194
SamplesHG01438, HG01468
Known GenesTHSD4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636853
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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