A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520221



Internal ID15447514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:145751008..145777369hg38UCSC Ensembl
InnerchrX:144832526..144858887hg19UCSC Ensembl
InnerchrX:144640218..144666579hg18UCSC Ensembl
InnerchrX:144538072..144564433hg17UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg3826362
hg1926362
hg1826362
hg1726362
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv679348, nssv661973
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520221
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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