A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519896



Internal ID15447189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:117028614..117056015hg38UCSC Ensembl
InnerchrX:116162582..116189983hg19UCSC Ensembl
InnerchrX:116046610..116074011hg18UCSC Ensembl
InnerchrX:115944464..115971865hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3827402
hg1927402
hg1827402
hg1727402
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv683424, nssv659376
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519896
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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