A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559289



Internal ID18857570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:55621512..55641775hg38UCSC Ensembl
Innerchr16:55655424..55675687hg19UCSC Ensembl
Innerchr16:54212925..54233188hg18UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3820264
hg1920264
hg1820264
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1064107
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)nssv3559289
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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