A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066586



Internal ID19155805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32233140..32732148hg38UCSC Ensembl
Innerchr16:32244461..32743469hg19UCSC Ensembl
Innerchr16:32151962..32650970hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38499009
hg19499009
hg18499009
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2852n100
Supporting Variantsnssv3550495, nssv3550493, nssv3716335, nssv3550491, nssv3550494, nssv3550492
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)nsv1066586
Frequency
Sample Size11257
Observed Gain4
Observed Loss2
Observed Complex0
Frequencyn/a


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