A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636761



Internal ID7023555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65805561..65811347hg38UCSC Ensembl
Innerchr15:65805561..65811347hg38UCSC Ensembl
Outerchr15:65805227..65811650hg38UCSC Ensembl
chr15:66097899..66103685hg19UCSC Ensembl
Innerchr15:66097899..66103685hg19UCSC Ensembl
Outerchr15:66097565..66103988hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg385787
hg195787
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15272861, essv15272860, essv15272873, essv15272876, essv15272857, essv15272885, essv15272872, essv15272880, essv15272858, essv15272879, essv15272859, essv15272870, essv15272875, essv15272855, essv15272856, essv15272867, essv15272862, essv15272868, essv15272883, essv15272863, essv15272866, essv15272878, essv15272881, essv15272877, essv15272864, essv15272871, essv15272869, essv15272865, essv15272882, essv15272884, essv15272874
SamplesHG03514, NA18924, HG03517, HG00640, NA18486, NA19190, HG03074, HG01168, HG02860, HG02981, HG03209, HG01069, NA19235, HG01048, HG03073, NA18908, NA19200, HG00731, HG02554, HG03457, HG02976, NA18858, HG01190, HG03433, HG02580, HG03419, HG02558, HG03103, HG02107, HG02013, HG01111
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636761
Frequency
Sample Size2504
Observed Gain0
Observed Loss31
Observed Complex0
Frequencyn/a


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