A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520288



Internal ID15447581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:149232993..149255678hg38UCSC Ensembl
Innerchr3:148950780..148973465hg19UCSC Ensembl
Innerchr3:150433470..150456155hg18UCSC Ensembl
Innerchr3:150433478..150456163hg17UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3822686
hg1922686
hg1822686
hg1722686
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv301n21
Supporting Variantsnssv697327
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520288
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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