A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055377



Internal ID19144596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32217659..33086089hg38UCSC Ensembl
Innerchr16:32228980..33097410hg19UCSC Ensembl
Innerchr16:32136481..33004911hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38868431
hg19868431
hg18868431
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2847n100
Supporting Variantsnssv3550447, nssv3550442, nssv3550444, nssv3550443, nssv3550448, nssv3550445, nssv3550446, nssv3550441
Samples
Known GenesLOC390705, 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)nsv1055377
Frequency
Sample Size11257
Observed Gain4
Observed Loss4
Observed Complex0
Frequencyn/a


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