A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569997



Internal ID16010720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:75672828..75699110hg38UCSC Ensembl
Innerchr15:75965169..75991451hg19UCSC Ensembl
Innerchr15:73752224..73778506hg18UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3826283
hg1926283
hg1826283
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv845291
Samples
Known GenesCSPG4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569997
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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