A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv859074



Internal ID15806344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:68607485..68678827hg38UCSC Ensembl
Innerchr16:68641388..68712730hg19UCSC Ensembl
Innerchr16:67198889..67270231hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3871343
hg1971343
hg1871343
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv572909
Supporting Variants
Samples
Known GenesCDH3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv859074
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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