A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570000



Internal ID16357409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:76043560..76053164hg38UCSC Ensembl
Innerchr15:76335901..76345505hg19UCSC Ensembl
Innerchr15:74122956..74132560hg18UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg389605
hg199605
hg189605
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4628n54
Supporting Variantsnssv845294
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570000
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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