A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv858145



Internal ID15805415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:58029609..58119987hg38UCSC Ensembl
Innerchr16:58063513..58153891hg19UCSC Ensembl
Innerchr16:56621014..56711392hg18UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg3890379
hg1990379
hg1890379
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv572760
Supporting Variants
Samples
Known GenesC16orf80, MMP15
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv858145
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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