A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057138



Internal ID19146357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32197413..32832367hg38UCSC Ensembl
Innerchr16:32208734..32843688hg19UCSC Ensembl
Innerchr16:32116235..32751189hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38634955
hg19634955
hg18634955
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2854n100
Supporting Variantsnssv3550394
Samples
Known GenesLOC390705, 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)nsv1057138
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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