A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517809



Internal ID15445102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:114455270..114565458hg38UCSC Ensembl
InnerchrX:113689723..113799907hg19UCSC Ensembl
InnerchrX:113595979..113706163hg18UCSC Ensembl
InnerchrX:113512703..113622887hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38110189
hg19110185
hg18110185
hg17110185
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695214
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517809
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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