A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv652239



Internal ID15042205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:68057555..68132927hg38UCSC Ensembl
Innerchr15:68349893..68425265hg19UCSC Ensembl
Innerchr15:66136947..66212319hg18UCSC Ensembl
Innerchr15:66136947..66212319hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3875373
hg1975373
hg1875373
hg1775373
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517512
Supporting Variants
Samples
Known GenesPIAS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv652239
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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