A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065083



Internal ID19154302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32169453..32938920hg38UCSC Ensembl
Innerchr16:32180774..32950241hg19UCSC Ensembl
Innerchr16:32088275..32857742hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38769468
hg19769468
hg18769468
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2841n100
Supporting Variantsnssv3550377, nssv3550376
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)nsv1065083
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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