A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv855489



Internal ID15802759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:29676801..29680638hg38UCSC Ensembl
Innerchr16:29688122..29691959hg19UCSC Ensembl
Innerchr16:29595623..29599460hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg383838
hg193838
hg183838
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571816
Supporting Variants
Samples
Known GenesQPRT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv855489
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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