A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038816



Internal ID18781347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:78504092..78588745hg38UCSC Ensembl
Innerchr15:78796434..78881087hg19UCSC Ensembl
Innerchr15:76583489..76668142hg18UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3884654
hg1984654
hg1884654
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3554591
Samples
Known GenesCHRNA5, HYKK, PSMA4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038816
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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