A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527225



Internal ID15454518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:70356324..70377916hg38UCSC Ensembl
Innerchr3:70405475..70427067hg19UCSC Ensembl
Innerchr3:70488165..70509757hg18UCSC Ensembl
Innerchr3:70488165..70509757hg17UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3821593
hg1921593
hg1821593
hg1721593
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703625
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527225
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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