A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059450



Internal ID19148669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:63257454..63362456hg38UCSC Ensembl
Innerchr16:63291358..63396360hg19UCSC Ensembl
Innerchr16:61848859..61953861hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38105003
hg19105003
hg18105003
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2991n100
Supporting Variantsnssv3559376, nssv3559378, nssv3559377, nssv3559375
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059450
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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