A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519045



Internal ID15446338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:86918470..86957790hg38UCSC Ensembl
InnerchrX:86173473..86212793hg19UCSC Ensembl
InnerchrX:86060129..86099449hg18UCSC Ensembl
InnerchrX:85979618..86018938hg17UCSC Ensembl
CytobandXq21.2
Allele length
AssemblyAllele length
hg3839321
hg1939321
hg1839321
hg1739321
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694301
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519045
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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