A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669959



Internal ID9936064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:71589277..71590883hg38UCSC Ensembl
Outerchr15:71588906..71591253hg38UCSC Ensembl
Innerchr15:71881616..71883222hg19UCSC Ensembl
Outerchr15:71881245..71883592hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg382348
hg192348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6541411, essv5559360, essv5722866, essv6276347, essv6449201, essv6426386, essv6578524, essv5463749, essv6388038, essv5482400, essv5525505, essv6585994, essv5765624, essv6500659, essv5931661, essv5859895, essv6456321, essv6311167, essv6209744, essv6337852, essv6107287, essv5785620, essv6565526
SamplesHG01060, HG01098, HG00640, HG00737, HG01070, HG00736, HG01083, HG01080, HG01072, HG01176, HG00731, HG01187, HG00740, HG01197, HG01101, HG01107, HG01075, HG00638, HG01174, HG01097, HG00554, HG01061, HG00553
Known GenesTHSD4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669959
Frequency
Sample Size1151
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


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