A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062675



Internal ID18805206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32233140..33813659hg38UCSC Ensembl
Innerchr16:32244461..33616126hg19UCSC Ensembl
Innerchr16:32151962..33523627hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381580520
hg191371666
hg181371666
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2839n100
Supporting Variantsnssv3716337
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)nsv1062675
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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