A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051459



Internal ID19140678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:68660771..68694098hg38UCSC Ensembl
Innerchr13:69234903..69268230hg19UCSC Ensembl
Innerchr13:68132904..68166231hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3833328
hg1933328
hg1833328
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1705n100
Supporting Variantsnssv3527953
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)nsv1051459
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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