A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522515



Internal ID20895876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:4808803..4811939hg38UCSC Ensembl
chr20:4789449..4792585hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg383137
hg193137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068924
Samples
Known GenesRASSF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522515
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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