A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525462



Internal ID15106069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:73057292..73271154hg38UCSC Ensembl
Innerchr15:73349633..73563495hg19UCSC Ensembl
Innerchr15:71136686..71350548hg18UCSC Ensembl
Innerchr15:71136686..71350548hg17UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38213863
hg19213863
hg18213863
hg17213863
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701590
Samples
Known GenesNEO1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525462
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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