A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516639



Internal ID15097246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:61882935..62047927hg38UCSC Ensembl
Innerchr15:62175134..62340126hg19UCSC Ensembl
Innerchr15:59962426..60127418hg18UCSC Ensembl
Innerchr15:59962426..60127418hg17UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38164993
hg19164993
hg18164993
hg17164993
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv152n21
Supporting Variantsnssv696714, nssv673394, nssv694350, nssv699374, nssv669799
Samples
Known GenesVPS13C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516639
Frequency
Sample Size2026
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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