A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526479



Internal ID15453772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:142381661..142472390hg38UCSC Ensembl
InnerchrX:141469447..141560176hg19UCSC Ensembl
InnerchrX:141297113..141387842hg18UCSC Ensembl
InnerchrX:141194967..141285696hg17UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg3890730
hg1990730
hg1890730
hg1790730
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702787
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526479
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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