A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060953



Internal ID19150172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70090445..70200621hg38UCSC Ensembl
Innerchr16:70124348..70234524hg19UCSC Ensembl
Innerchr16:68681849..68792025hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38110177
hg19110177
hg18110177
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559528, nssv3559527
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)nsv1060953
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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