A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636799



Internal ID7023593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68027533..68028703hg38UCSC Ensembl
Innerchr15:68027538..68028698hg38UCSC Ensembl
Outerchr15:68027528..68028708hg38UCSC Ensembl
chr15:68319871..68321041hg19UCSC Ensembl
Innerchr15:68319876..68321036hg19UCSC Ensembl
Outerchr15:68319866..68321046hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381171
hg191171
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15279376, essv15279378, essv15279379, essv15279377, essv15279380
SamplesHG03126, NA19036, NA18934, HG01879, NA19117
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636799
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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