A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056893



Internal ID19146112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32169453..32481160hg38UCSC Ensembl
Innerchr16:32180774..32492481hg19UCSC Ensembl
Innerchr16:32088275..32399982hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38311708
hg19311708
hg18311708
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2855n100
Supporting Variantsnssv3550361
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)nsv1056893
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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