A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569970



Internal ID16357379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:73724281..73766740hg38UCSC Ensembl
Innerchr15:74016622..74059081hg19UCSC Ensembl
Innerchr15:71803675..71846134hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3842460
hg1942460
hg1842460
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv845259, nssv845258
Samples
Known GenesC15orf59
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569970
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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