A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14245321



Internal ID21303024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:21525404..21569910hg38UCSC Ensembl
Outerchr16:21522983..21574471hg38UCSC Ensembl
Innerchr16:21536725..21581231hg19UCSC Ensembl
Outerchr16:21534304..21585792hg19UCSC Ensembl
Innerchr16:21444226..21488732hg18UCSC Ensembl
Outerchr16:21441805..21493293hg18UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg3851489
hg1951489
hg1851489
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169963
Supporting Variants
SamplesMLY_3
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14245321
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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