A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515589



Internal ID15443200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:109255875..109288350hg38UCSC Ensembl
Innerchr8:110268104..110300579hg19UCSC Ensembl
Innerchr8:110337280..110369755hg18UCSC Ensembl
Innerchr8:110337280..110369755hg17UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg3832476
hg1932476
hg1832476
hg1732476
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv665886, nssv664016, nssv669986, nssv680099, nssv690468
Samples
Known GenesNUDCD1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515589
Frequency
Sample Size2026
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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