A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518044



Internal ID15098651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113004794..113211022hg38UCSC Ensembl
Innerchr13:113659108..113865336hg19UCSC Ensembl
Innerchr13:112707109..112913337hg18UCSC Ensembl
Innerchr13:112707109..112913337hg17UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38206229
hg19206229
hg18206229
hg17206229
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695455
Samples
Known GenesCUL4A, F10, F7, MCF2L, PCID2, PROZ
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518044
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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