A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065897



Internal ID19155116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32169453..32513445hg38UCSC Ensembl
Innerchr16:32180774..32524766hg19UCSC Ensembl
Innerchr16:32088275..32432267hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38343993
hg19343993
hg18343993
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2853n100
Supporting Variantsnssv3550362
Samples
Known GenesLOC390705, TP53TG3D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065897
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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