A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527835



Internal ID15455128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:113202539..113312851hg38UCSC Ensembl
InnerchrX:112445766..112556078hg19UCSC Ensembl
InnerchrX:112332422..112442734hg18UCSC Ensembl
InnerchrX:112251911..112362223hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38110313
hg19110313
hg18110313
hg17110313
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704332
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527835
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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