A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517467



Internal ID15444760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:20052354..20054653hg38UCSC Ensembl
Innerchr20:20032998..20035297hg19UCSC Ensembl
Innerchr20:19980998..19983297hg18UCSC Ensembl
Innerchr20:19980998..19983297hg17UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg382300
hg192300
hg182300
hg172300
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv693939, nssv652346, nssv665497, nssv674983, nssv689179, nssv652102
Samples
Known GenesC20orf26, CRNKL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517467
Frequency
Sample Size2026
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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