A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056596



Internal ID18799127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32269023..33825347hg38UCSC Ensembl
Innerchr16:32280344..33627814hg19UCSC Ensembl
Innerchr16:32187845..33535315hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381556325
hg191347471
hg181347471
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2839n100
Supporting Variantsnssv3550564
Samples
Known GenesLOC390705, RNU6-76P, SLC6A10P, 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)nsv1056596
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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