A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523201



Internal ID15450494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:115942186..115970664hg38UCSC Ensembl
InnerchrX:115058519..115086997hg19UCSC Ensembl
InnerchrX:114972547..115001025hg18UCSC Ensembl
InnerchrX:114870401..114898879hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3828479
hg1928479
hg1828479
hg1728479
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698920
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523201
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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