A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570023



Internal ID16357432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:76591786..76685798hg38UCSC Ensembl
Innerchr15:76884127..76978139hg19UCSC Ensembl
Innerchr15:74671182..74765194hg18UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3894013
hg1994013
hg1894013
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4633n54
Supporting Variantsnssv845372
Samples
Known GenesSCAPER
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570023
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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