A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526134



Internal ID15453427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:116458613..116600548hg38UCSC Ensembl
InnerchrX:115589779..115734516hg19UCSC Ensembl
InnerchrX:115503807..115618544hg18UCSC Ensembl
InnerchrX:115401661..115516398hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38141936
hg19144738
hg18114738
hg17114738
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv526n21
Supporting Variantsnssv702388
Samples
Known GenesCXorf61, SLC6A14
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526134
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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