A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521194



Internal ID15448487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:28241793..28294683hg38UCSC Ensembl
InnerchrX:28259910..28312800hg19UCSC Ensembl
InnerchrX:28169831..28222721hg18UCSC Ensembl
InnerchrX:28019567..28072457hg17UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg3852891
hg1952891
hg1852891
hg1752891
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697837
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521194
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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