A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055280



Internal ID19144499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32022053..33730031hg38UCSC Ensembl
Innerchr16:32033374..33532498hg19UCSC Ensembl
Innerchr16:31940875..33439999hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381707979
hg191499125
hg181499125
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2844n100
Supporting Variantsnssv3549220, nssv3549221
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)nsv1055280
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer