A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636717



Internal ID7023511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63470912..63472776hg38UCSC Ensembl
Innerchr15:63470912..63472776hg38UCSC Ensembl
Outerchr15:63470735..63472891hg38UCSC Ensembl
chr15:63763111..63764975hg19UCSC Ensembl
Innerchr15:63763111..63764975hg19UCSC Ensembl
Outerchr15:63762934..63765090hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg381865
hg191865
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15270978
SamplesHG01794
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636717
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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