A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv858696



Internal ID16152652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:58614411..58619934hg38UCSC Ensembl
Innerchr16:58648315..58653838hg19UCSC Ensembl
Innerchr16:57205816..57211339hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg385524
hg195524
hg185524
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv572787
Supporting Variants
Samples
Known GenesCNOT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv858696
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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