A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv502n21



Internal ID20132223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:14591881..14702502hg38UCSC Ensembl
chrX:14610003..14720624hg19UCSC Ensembl
chrX:14519924..14630545hg18UCSC Ensembl
chrX:14369660..14480281hg17UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38110622
hg19110622
hg18110622
hg17110622
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv518237, nsv518884
Samples
Known GenesGLRA2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv502n21
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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