A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526428



Internal ID15107035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:116458613..116493797hg38UCSC Ensembl
InnerchrX:115589779..115624958hg19UCSC Ensembl
InnerchrX:115503807..115538986hg18UCSC Ensembl
InnerchrX:115401661..115436840hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3835185
hg1935180
hg1835180
hg1735180
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702730
Samples
Known GenesCXorf61, SLC6A14
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526428
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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