A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559367



Internal ID18857648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:60583413..60617994hg38UCSC Ensembl
Innerchr16:60617317..60651898hg19UCSC Ensembl
Innerchr16:59174818..59209399hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3834582
hg1934582
hg1834582
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1057340
Supporting Variants
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)nssv3559367
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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