A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518553



Internal ID15445846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:106577450..106587366hg38UCSC Ensembl
Innerchr13:107229798..107239714hg19UCSC Ensembl
Innerchr13:106027799..106037715hg18UCSC Ensembl
Innerchr13:106027799..106037715hg17UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg389917
hg199917
hg189917
hg179917
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695996
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518553
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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