A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523582



Internal ID15104189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:116269375..116491109hg38UCSC Ensembl
InnerchrX:115400631..115622273hg19UCSC Ensembl
InnerchrX:115314659..115536301hg18UCSC Ensembl
InnerchrX:115212513..115434155hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38221735
hg19221643
hg18221643
hg17221643
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699371
Samples
Known GenesCXorf61, SLC6A14
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523582
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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