A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056337



Internal ID18798868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32233140..33908301hg38UCSC Ensembl
Innerchr16:32244461..33710768hg19UCSC Ensembl
Innerchr16:32151962..33618269hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381675162
hg191466308
hg181466308
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2840n100
Supporting Variantsnssv3716338
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)nsv1056337
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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