A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528471



Internal ID15109078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:90008292..90066698hg38UCSC Ensembl
Innerchr1:90473851..90532256hg19UCSC Ensembl
Innerchr1:90246439..90304844hg18UCSC Ensembl
Innerchr1:90185872..90244277hg17UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg3858407
hg1958406
hg1858406
hg1758406
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705074
Samples
Known GenesZNF326
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528471
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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