A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527390



Internal ID15454683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:35463707..35546141hg38UCSC Ensembl
InnerchrX:35481824..35564258hg19UCSC Ensembl
InnerchrX:35391745..35474179hg18UCSC Ensembl
InnerchrX:35241481..35323915hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3882435
hg1982435
hg1882435
hg1782435
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703825
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527390
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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