A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525867



Internal ID15106474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:138498822..139357684hg38UCSC Ensembl
InnerchrX:137580983..138439843hg19UCSC Ensembl
InnerchrX:137408649..138267509hg18UCSC Ensembl
InnerchrX:137306503..138165363hg17UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38858863
hg19858861
hg18858861
hg17858861
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702066
Samples
Known GenesFGF13, FGF13-AS1, LINC00889, MIR504
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525867
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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