A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063059



Internal ID19152278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32016645..33952512hg38UCSC Ensembl
Innerchr16:32027966..33754979hg19UCSC Ensembl
Innerchr16:31935467..33662480hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381935868
hg191727014
hg181727014
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2844n100
Supporting Variantsnssv3549196, nssv3716196, nssv3549197
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)nsv1063059
Frequency
Sample Size11257
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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