A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526224



Internal ID15106831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:151003841..151070675hg38UCSC Ensembl
Innerchr5:150383403..150450236hg19UCSC Ensembl
Innerchr5:150363596..150430429hg18UCSC Ensembl
Innerchr5:150363596..150430429hg17UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3866835
hg1966834
hg1866834
hg1766834
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702490
Samples
Known GenesGPX3, TNIP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526224
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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