A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636722



Internal ID7023516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63884722..63887623hg38UCSC Ensembl
Innerchr15:63884725..63887620hg38UCSC Ensembl
Outerchr15:63884719..63887626hg38UCSC Ensembl
chr15:64176921..64179822hg19UCSC Ensembl
Innerchr15:64176924..64179819hg19UCSC Ensembl
Outerchr15:64176918..64179825hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg382902
hg192902
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15271222
SamplesHG01956
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636722
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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