A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149339



Internal ID15532196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:84579799..84639929hg38UCSC Ensembl
Innerchr16:84613405..84673535hg19UCSC Ensembl
Innerchr16:83170906..83231036hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3860131
hg1960131
hg1860131
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573464
Supporting Variants
SamplesHGDP01273
Known GenesCOTL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149339
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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