A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056035



Internal ID19145254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:33086089..33822829hg38UCSC Ensembl
Innerchr16:33097410..33625296hg19UCSC Ensembl
Innerchr16:33004911..33532797hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38736741
hg19527887
hg18527887
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552485
Samples
Known GenesLOC390705, RNU6-76P, 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)nsv1056035
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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