A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060755



Internal ID19149974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:33024675..34034322hg38UCSC Ensembl
Innerchr16:33035996..33836789hg19UCSC Ensembl
Innerchr16:32943497..33744290hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381009648
hg19800794
hg18800794
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2905n100
Supporting Variantsnssv3717244
Samples
Known GenesLOC390705, RNU6-76P, TP53TG3, TP53TG3B, TP53TG3C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060755
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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