A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059016



Internal ID18801547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32233140..34035419hg38UCSC Ensembl
Innerchr16:32244461..33837886hg19UCSC Ensembl
Innerchr16:32151962..33745387hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381802280
hg191593426
hg181593426
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2840n100
Supporting Variantsnssv3716339, nssv3550514
Samples
Known GenesLOC390705, RNU6-76P, SLC6A10P, TP53TG3, TP53TG3B, TP53TG3C, TP53TG3D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059016
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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