A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063341



Internal ID19152560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70117612..70212505hg38UCSC Ensembl
Innerchr16:70151515..70246408hg19UCSC Ensembl
Innerchr16:68709016..68803909hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3894894
hg1994894
hg1894894
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3013n100
Supporting Variantsnssv3559539, nssv3719009, nssv3719006, nssv3559533, nssv3719010, nssv3719007, nssv3559535, nssv3559537, nssv3719005, nssv3559536, nssv3719012, nssv3719008, nssv3559538, nssv3719013, nssv3719011, nssv3559534
Samples
Known GenesCLEC18C, PDPR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063341
Frequency
Sample Size11257
Observed Gain16
Observed Loss0
Observed Complex0
Frequencyn/a


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