A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526897



Internal ID15107504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:23668070..23683545hg38UCSC Ensembl
InnerchrX:23686187..23701662hg19UCSC Ensembl
InnerchrX:23596108..23611583hg18UCSC Ensembl
InnerchrX:23445844..23461319hg17UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3815476
hg1915476
hg1815476
hg1715476
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703255
Samples
Known GenesPRDX4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526897
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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