A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518818



Internal ID15446111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:122393524..122404977hg38UCSC Ensembl
InnerchrX:121527377..121538830hg19UCSC Ensembl
InnerchrX:121355058..121366511hg18UCSC Ensembl
InnerchrX:121252912..121264365hg17UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3811454
hg1911454
hg1811454
hg1711454
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696271
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518818
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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