A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636996



Internal ID7023790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79229745..79230137hg38UCSC Ensembl
Innerchr15:79229751..79230131hg38UCSC Ensembl
Outerchr15:79229739..79230143hg38UCSC Ensembl
chr15:79522087..79522479hg19UCSC Ensembl
Innerchr15:79522093..79522473hg19UCSC Ensembl
Outerchr15:79522081..79522485hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38393
hg19393
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15302777, essv15302774, essv15302773, essv15302776, essv15302775
SamplesNA19394, NA19207, HG03634, NA19440, HG02343
Known GenesLOC729911
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636996
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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