A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523486



Internal ID15450779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:116016501..116081958hg38UCSC Ensembl
InnerchrX:115132834..115213211hg19UCSC Ensembl
InnerchrX:115046862..115127239hg18UCSC Ensembl
InnerchrX:114944716..115025093hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3865458
hg1980378
hg1880378
hg1780378
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699253
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523486
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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