A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3549385



Internal ID18500980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32081501..33043325hg38UCSC Ensembl
Innerchr16:32092822..33054646hg19UCSC Ensembl
Innerchr16:32000323..32962147hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38961825
hg19961825
hg18961825
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058069
Supporting Variants
Samples
Known GenesHERC2P4, LOC390705, 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)nssv3549385
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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