A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525975



Internal ID15453268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:98068833..98153530hg38UCSC Ensembl
InnerchrX:97323831..97408528hg19UCSC Ensembl
InnerchrX:97210487..97295184hg18UCSC Ensembl
InnerchrX:97129976..97214673hg17UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg3884698
hg1984698
hg1884698
hg1784698
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702193
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525975
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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