A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527473



Internal ID15454766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:148549073..148619463hg38UCSC Ensembl
InnerchrX:147630594..147700984hg19UCSC Ensembl
InnerchrX:147438286..147508676hg18UCSC Ensembl
InnerchrX:147336140..147406530hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3870391
hg1970391
hg1870391
hg1770391
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703916
Samples
Known GenesAFF2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527473
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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