A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520550



Internal ID15101157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:131294015..131355743hg38UCSC Ensembl
InnerchrX:130427989..130489717hg19UCSC Ensembl
InnerchrX:130255670..130317398hg18UCSC Ensembl
InnerchrX:130153524..130215252hg17UCSC Ensembl
CytobandXq26.1
Allele length
AssemblyAllele length
hg3861729
hg1961729
hg1861729
hg1761729
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv687736, nssv672464, nssv701310, nssv686887
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520550
Frequency
Sample Size2026
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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