A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559379



Internal ID18857660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:63257454..63367393hg38UCSC Ensembl
Innerchr16:63291358..63401297hg19UCSC Ensembl
Innerchr16:61848859..61958798hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38109940
hg19109940
hg18109940
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055520
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)nssv3559379
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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