A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059013



Internal ID19148232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:65327036..65428955hg38UCSC Ensembl
Innerchr16:65360939..65462858hg19UCSC Ensembl
Innerchr16:63918440..64020359hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38101920
hg19101920
hg18101920
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2994n100
Supporting Variantsnssv3559437
Samples
Known GenesLINC00922
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059013
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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