A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518316



Internal ID15098923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:73998652..74038742hg38UCSC Ensembl
Innerchr15:74290993..74331083hg19UCSC Ensembl
Innerchr15:72078046..72118136hg18UCSC Ensembl
Innerchr15:72078046..72118136hg17UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3840091
hg1940091
hg1840091
hg1740091
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695747
Samples
Known GenesPML
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518316
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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