A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv690879



Internal ID15427531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:114479187..114537428hg38UCSC Ensembl
InnerchrX:113713640..113771881hg19UCSC Ensembl
InnerchrX:113619896..113678137hg18UCSC Ensembl
InnerchrX:113536620..113594861hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3858242
hg1958242
hg1858242
hg1758242
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520153
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv690879
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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