A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516129



Internal ID15443422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:79138721..79153447hg38UCSC Ensembl
Innerchr15:79431063..79445789hg19UCSC Ensembl
Innerchr15:77218118..77232844hg18UCSC Ensembl
Innerchr15:77218118..77232844hg17UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3814727
hg1914727
hg1814727
hg1714727
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv659379, nssv652530
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516129
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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