A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518666



Internal ID15099273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:15418493..15420892hg38UCSC Ensembl
InnerchrX:15436616..15439015hg19UCSC Ensembl
InnerchrX:15346537..15348936hg18UCSC Ensembl
InnerchrX:15196273..15198672hg17UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg382400
hg192400
hg182400
hg172400
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696115
Samples
Known GenesPIR, PIR-FIGF
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518666
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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