A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048833



Internal ID18791364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:77002252..77046918hg38UCSC Ensembl
Innerchr15:77294593..77339260hg19UCSC Ensembl
Innerchr15:75081648..75126315hg18UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3844667
hg1944668
hg1844668
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3554585
Samples
Known GenesPSTPIP1, TSPAN3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048833
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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