A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv678486



Internal ID15415138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:70706792..70873743hg38UCSC Ensembl
InnerchrX:69926642..70093593hg19UCSC Ensembl
InnerchrX:69843367..70010318hg18UCSC Ensembl
InnerchrX:69709663..69876614hg17UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg38166952
hg19166952
hg18166952
hg17166952
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517078
Supporting Variants
Samples
Known GenesTEX11
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv678486
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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