A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059261



Internal ID19148480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32022053..32868451hg38UCSC Ensembl
Innerchr16:32033374..32879772hg19UCSC Ensembl
Innerchr16:31940875..32787273hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38846399
hg19846399
hg18846399
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2847n100
Supporting Variantsnssv3549215, nssv3716203
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)nsv1059261
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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