A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518237



Internal ID15098844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:14591881..14674129hg38UCSC Ensembl
InnerchrX:14610003..14692251hg19UCSC Ensembl
InnerchrX:14519924..14602172hg18UCSC Ensembl
InnerchrX:14369660..14451908hg17UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3882249
hg1982249
hg1882249
hg1782249
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv502n21
Supporting Variantsnssv695666
Samples
Known GenesGLRA2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518237
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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