A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050884



Internal ID18793415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:74102642..74197072hg38UCSC Ensembl
Innerchr15:74394983..74489413hg19UCSC Ensembl
Innerchr15:72182036..72276466hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3894431
hg1994431
hg1894431
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3717960
Samples
Known GenesISLR, ISLR2, LOC283731, STRA6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050884
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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