A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570001



Internal ID16357410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:76043560..76053246hg38UCSC Ensembl
Innerchr15:76335901..76345587hg19UCSC Ensembl
Innerchr15:74122956..74132642hg18UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg389687
hg199687
hg189687
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4628n54
Supporting Variantsnssv845298, nssv845295, nssv845297, nssv845296
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570001
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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