A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522625



Internal ID15103232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:14501748..14615051hg38UCSC Ensembl
InnerchrX:14519870..14633173hg19UCSC Ensembl
InnerchrX:14429791..14543094hg18UCSC Ensembl
InnerchrX:14279527..14392830hg17UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38113304
hg19113304
hg18113304
hg17113304
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv706022
Samples
Known GenesGLRA2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522625
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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