A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv659850



Internal ID15049816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31728323..32655605hg38UCSC Ensembl
Innerchr15:32020526..32947806hg19UCSC Ensembl
Innerchr15:29807818..30735098hg18UCSC Ensembl
Innerchr15:29807818..30735098hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38927283
hg19927281
hg18927281
hg17927281
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517740
Supporting Variants
Samples
Known GenesARHGAP11A, CHRNA7, GOLGA8K, GOLGA8O, GOLGA8R, LOC100996255, SCG5, ULK4P1, ULK4P2, ULK4P3, WHAMMP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv659850
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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