A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636806



Internal ID7023600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68545568..68548290hg38UCSC Ensembl
Innerchr15:68545568..68548290hg38UCSC Ensembl
Outerchr15:68545382..68548490hg38UCSC Ensembl
chr15:68837907..68840629hg19UCSC Ensembl
Innerchr15:68837907..68840629hg19UCSC Ensembl
Outerchr15:68837721..68840829hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg382723
hg192723
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15279460, essv15279463, essv15279461, essv15279464, essv15279466, essv15279459, essv15279465, essv15279462, essv15279467
SamplesHG03247, HG03241, HG03069, HG02541, HG03073, HG03054, NA18856, HG03240, HG03025
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636806
Frequency
Sample Size2504
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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