A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517490



Internal ID15444783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:11890981..11904456hg38UCSC Ensembl
Innerchr3:11932455..11945930hg19UCSC Ensembl
Innerchr3:11907455..11920930hg18UCSC Ensembl
Innerchr3:11907455..11920930hg17UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg3813476
hg1913476
hg1813476
hg1713476
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv672769, nssv652179
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517490
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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