A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526373



Internal ID15453666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:56363151..56363408hg38UCSC Ensembl
Innerchr20:54938207..54938464hg19UCSC Ensembl
Innerchr20:54371614..54371871hg18UCSC Ensembl
Innerchr20:54371614..54371871hg17UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38258
hg19258
hg18258
hg17258
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702669
Samples
Known GenesFAM210B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526373
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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