A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14246165



Internal ID21310798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:23813525..23935968hg38UCSC Ensembl
Outerchr16:23811667..23938591hg38UCSC Ensembl
Innerchr16:23824846..23947289hg19UCSC Ensembl
Outerchr16:23822988..23949912hg19UCSC Ensembl
Innerchr16:23732347..23854790hg18UCSC Ensembl
Outerchr16:23730489..23857413hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38126925
hg19126925
hg18126925
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170092
Supporting Variants
SamplesPML_1
Known GenesPRKCB
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14246165
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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