A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3547731



Internal ID18499326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32166460..32478247hg38UCSC Ensembl
Innerchr15:32458661..32770448hg19UCSC Ensembl
Innerchr15:30245953..30557740hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38311788
hg19311788
hg18311788
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036895
Supporting Variants
Samples
Known GenesCHRNA7, GOLGA8K, GOLGA8O, ULK4P1, ULK4P2, ULK4P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3547731
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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