A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522197



Internal ID15449490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:56348706..56362487hg38UCSC Ensembl
Innerchr20:54923762..54937543hg19UCSC Ensembl
Innerchr20:54357169..54370950hg18UCSC Ensembl
Innerchr20:54357169..54370950hg17UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3813782
hg1913782
hg1813782
hg1713782
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694970
Samples
Known GenesFAM210B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522197
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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