A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518364



Internal ID15098971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:2807348..2820763hg38UCSC Ensembl
Innerchr20:2787994..2801409hg19UCSC Ensembl
Innerchr20:2735994..2749409hg18UCSC Ensembl
Innerchr20:2735994..2749409hg17UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3813416
hg1913416
hg1813416
hg1713416
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695791
Samples
Known GenesC20orf141, TMEM239
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518364
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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