A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517873



Internal ID8412148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:43545579..43678961hg38UCSC Ensembl
InnerchrX:43404827..43538209hg19UCSC Ensembl
InnerchrX:43289771..43423153hg18UCSC Ensembl
InnerchrX:43161081..43294463hg17UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38133383
hg19133383
hg18133383
hg17133383
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695279
Samples
Known GenesMAOA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517873
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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