A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3542775



Internal ID18841056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:19928432..19959156hg38UCSC Ensembl
Innerchr16:19939754..19970478hg19UCSC Ensembl
Innerchr16:19847255..19877979hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3830725
hg1930725
hg1830725
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046481
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)nssv3542775
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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