A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570021



Internal ID16357430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:76521579..76685798hg38UCSC Ensembl
Innerchr15:76813920..76978139hg19UCSC Ensembl
Innerchr15:74600975..74765194hg18UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg38164220
hg19164220
hg18164220
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4632n54
Supporting Variantsnssv845367, nssv845370, nssv845366, nssv845369, nssv845368
Samples
Known GenesSCAPER
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570021
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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