A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636942



Internal ID7023736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:76494914..76498937hg38UCSC Ensembl
Innerchr15:76494914..76498937hg38UCSC Ensembl
Outerchr15:76494622..76499146hg38UCSC Ensembl
chr15:76787255..76791278hg19UCSC Ensembl
Innerchr15:76787255..76791278hg19UCSC Ensembl
Outerchr15:76786963..76791487hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg384024
hg194024
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15295770, essv15295769, essv15295772, essv15295771
SamplesHG03126, HG03385, HG02334, HG01377
Known GenesSCAPER
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636942
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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