A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636015



Internal ID7022811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:29460764..29463441hg38UCSC Ensembl
Innerchr15:29460764..29463441hg38UCSC Ensembl
Outerchr15:29460512..29463746hg38UCSC Ensembl
chr15:29752968..29755645hg19UCSC Ensembl
Innerchr15:29752968..29755645hg19UCSC Ensembl
Outerchr15:29752716..29755950hg19UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg382678
hg192678
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15203044, essv15203043, essv15203045
SamplesHG01066, HG01069, HG01055
Known GenesFAM189A1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636015
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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