A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568915



Internal ID16356324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32673156..32701855hg38UCSC Ensembl
Innerchr15:32965357..32994056hg19UCSC Ensembl
Innerchr15:30752649..30781348hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3828700
hg1928700
hg1828700
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv839793
Samples
Known GenesSCG5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568915
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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