A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051809



Internal ID18794340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:43166264..43208745hg38UCSC Ensembl
Innerchr13:43740400..43782881hg19UCSC Ensembl
Innerchr13:42638400..42680881hg18UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3842482
hg1942482
hg1842482
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1642n100
Supporting Variantsnssv3523413, nssv3523414, nssv3523412, nssv3714975
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051809
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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