A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043959



Internal ID18786490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:11945489..12191412hg38UCSC Ensembl
Innerchr16:12039346..12285269hg19UCSC Ensembl
Innerchr16:11946847..12192770hg18UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38245924
hg19245924
hg18245924
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3557142
Samples
Known GenesSNX29, TNFRSF17
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043959
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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