A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050169



Internal ID18792700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:108300121..108874622hg38UCSC Ensembl
Innerchr13:108952469..109526970hg19UCSC Ensembl
Innerchr13:107750470..108324971hg18UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38574502
hg19574502
hg18574502
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3713303
Samples
Known GenesMYO16, TNFSF13B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050169
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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