A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059272



Internal ID18801803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32169453..33043325hg38UCSC Ensembl
Innerchr16:32180774..33054646hg19UCSC Ensembl
Innerchr16:32088275..32962147hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38873873
hg19873873
hg18873873
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2837n100
Supporting Variantsnssv3550378
Samples
Known GenesLOC390705, 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)nsv1059272
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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