A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526507



Internal ID15453800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:4813032..4815057hg38UCSC Ensembl
Innerchr20:4793678..4795703hg19UCSC Ensembl
Innerchr20:4741678..4743703hg18UCSC Ensembl
Innerchr20:4741678..4743703hg17UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg382026
hg192026
hg182026
hg172026
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702817
Samples
Known GenesRASSF2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526507
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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