A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057368



Internal ID19146587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32147274..32732148hg38UCSC Ensembl
Innerchr16:32158595..32743469hg19UCSC Ensembl
Innerchr16:32066096..32650970hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38584875
hg19584875
hg18584875
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2851n100
Supporting Variantsnssv3550340
Samples
Known GenesHERC2P4, LOC390705, 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)nsv1057368
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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