A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv153n21



Internal ID20131874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:70880359..71074673hg38UCSC Ensembl
chr15:71172698..71367012hg19UCSC Ensembl
chr15:68959752..69154066hg18UCSC Ensembl
chr15:68959752..69154066hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38194315
hg19194315
hg18194315
hg17194315
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv523555, nsv521336
Samples
Known GenesLRRC49, THAP10
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv153n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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