A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059842



Internal ID19149061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32022053..32623431hg38UCSC Ensembl
Innerchr16:32033374..32634752hg19UCSC Ensembl
Innerchr16:31940875..32542253hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38601379
hg19601379
hg18601379
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2836n100
Supporting Variantsnssv3549212, nssv3549211
Samples
Known GenesHERC2P4, LOC390705, TP53TG3D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059842
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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