A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15266865



Internal ID2320599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62413891..62415594hg38UCSC Ensembl
Innerchr15:62413891..62415594hg38UCSC Ensembl
Outerchr15:62413891..62415594hg38UCSC Ensembl
chr15:62706090..62707793hg19UCSC Ensembl
Innerchr15:62706090..62707793hg19UCSC Ensembl
Outerchr15:62706090..62707793hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg381704
hg191704
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636701
Supporting Variants
SamplesHG02067
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15266865
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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