A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061079



Internal ID18803610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32289569..33829351hg38UCSC Ensembl
Innerchr16:32300890..33631818hg19UCSC Ensembl
Innerchr16:32208391..33539319hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381539783
hg191330929
hg181330929
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2839n100
Supporting Variantsnssv3550603, nssv3716353
Samples
Known GenesLOC390705, RNU6-76P, SLC6A10P, TP53TG3, TP53TG3B, TP53TG3C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061079
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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