A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519242



Internal ID15446535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:98559306..98578777hg38UCSC Ensembl
InnerchrX:97814304..97833775hg19UCSC Ensembl
InnerchrX:97700960..97720431hg18UCSC Ensembl
InnerchrX:97620449..97639920hg17UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg3819472
hg1919472
hg1819472
hg1719472
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696735
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519242
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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