A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058311



Internal ID19147530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:84574421..84612073hg38UCSC Ensembl
Innerchr16:84608027..84645679hg19UCSC Ensembl
Innerchr16:83165528..83203180hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3837653
hg1937653
hg1837653
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3058n100
Supporting Variantsnssv3559957
Samples
Known GenesCOTL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058311
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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