A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636966



Internal ID7023760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77479673..77482826hg38UCSC Ensembl
Innerchr15:77479673..77482826hg38UCSC Ensembl
Outerchr15:77479449..77483072hg38UCSC Ensembl
chr15:77772015..77775168hg19UCSC Ensembl
Innerchr15:77772015..77775168hg19UCSC Ensembl
Outerchr15:77771791..77775414hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg383154
hg193154
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15300472, essv15300471
SamplesNA19734, HG01133
Known GenesHMG20A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636966
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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