A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3549344



Internal ID18500939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32069540..32944737hg38UCSC Ensembl
Innerchr16:32080861..32956058hg19UCSC Ensembl
Innerchr16:31988362..32863559hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38875198
hg19875198
hg18875198
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1064268
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)nssv3549344
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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