A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520414



Internal ID15447707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:96052219..96130594hg38UCSC Ensembl
InnerchrX:95307218..95385593hg19UCSC Ensembl
InnerchrX:95193874..95272249hg18UCSC Ensembl
InnerchrX:95113363..95191738hg17UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg3878376
hg1978376
hg1878376
hg1778376
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697401
Samples
Known GenesMIR548AE1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520414
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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