A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526364



Internal ID15453657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:45251387..45401909hg38UCSC Ensembl
InnerchrX:45110632..45261154hg19UCSC Ensembl
InnerchrX:44995576..45146098hg18UCSC Ensembl
InnerchrX:44866886..45017408hg17UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38150523
hg19150523
hg18150523
hg17150523
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702658
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526364
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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