A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035899



Internal ID18778430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:82439721..82646980hg38UCSC Ensembl
Innerchr15:83108446..83315731hg19UCSC Ensembl
Innerchr15:80905501..81112786hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38207260
hg19207286
hg18207286
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3718108
Samples
Known GenesCPEB1, CSPG4P8, LOC727751, LOC80154, RPS17, RPS17L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035899
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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