A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3555698



Internal ID18853979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:33724141..34208804hg38UCSC Ensembl
Innerchr16:33526608..34011271hg19UCSC Ensembl
Innerchr16:33434109..33918772hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38484664
hg19484664
hg18484664
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056975
Supporting Variants
Samples
Known GenesLINC00273, RNU6-76P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3555698
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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