A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523884



Internal ID15451177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:100535293..100580758hg38UCSC Ensembl
Innerchr15:101075498..101120963hg19UCSC Ensembl
Innerchr15:98893021..98938486hg18UCSC Ensembl
Innerchr15:98893021..98938486hg17UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3845466
hg1945466
hg1845466
hg1745466
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699726
Samples
Known GenesCERS3, LINS, PRKXP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523884
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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