A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520216



Internal ID15447509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:98113831..98354299hg38UCSC Ensembl
InnerchrX:97368829..97609297hg19UCSC Ensembl
InnerchrX:97255485..97495953hg18UCSC Ensembl
InnerchrX:97174974..97415442hg17UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg38240469
hg19240469
hg18240469
hg17240469
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv663635, nssv661937
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520216
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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