A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056671



Internal ID19145890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32047162..33952512hg38UCSC Ensembl
Innerchr16:32058483..33754979hg19UCSC Ensembl
Innerchr16:31965984..33662480hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381905351
hg191696497
hg181696497
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2844n100
Supporting Variantsnssv3549283, nssv3716229, nssv3549285, nssv3549284
Samples
Known GenesHERC2P4, LOC390705, RNU6-76P, SLC6A10P, 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)nsv1056671
Frequency
Sample Size11257
Observed Gain3
Observed Loss1
Observed Complex0
Frequencyn/a


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