A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522033



Internal ID15102640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:70233184..70245422hg38UCSC Ensembl
InnerchrX:69453034..69465272hg19UCSC Ensembl
InnerchrX:69369759..69381997hg18UCSC Ensembl
InnerchrX:69236055..69248293hg17UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3812239
hg1912239
hg1812239
hg1712239
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694802
Samples
Known GenesAWAT1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522033
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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