A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055520



Internal ID19144739
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 StatusM
Merged Variantsdgv2991n100
Supporting Variantsnssv3559379
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)nsv1055520
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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