A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520810



Internal ID15101417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:23036333..23036445hg38UCSC Ensembl
Innerchr20:23016970..23017082hg19UCSC Ensembl
Innerchr20:22964970..22965082hg18UCSC Ensembl
Innerchr20:22964970..22965082hg17UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38113
hg19113
hg18113
hg17113
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv675703, nssv686681, nssv676869
Samples
Known GenesSSTR4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520810
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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