A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527392



Internal ID15454685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:107510251..107539772hg38UCSC Ensembl
Innerchr13:108162599..108192120hg19UCSC Ensembl
Innerchr13:106960600..106990121hg18UCSC Ensembl
Innerchr13:106960600..106990121hg17UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3829522
hg1929522
hg1829522
hg1729522
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703827
Samples
Known GenesFAM155A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527392
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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