A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523224



Internal ID15450517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:146569201..146586273hg38UCSC Ensembl
InnerchrX:145650719..145667791hg19UCSC Ensembl
InnerchrX:145458411..145475483hg18UCSC Ensembl
InnerchrX:145356265..145373337hg17UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg3817073
hg1917073
hg1817073
hg1717073
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698946
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523224
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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