A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522705



Internal ID20896066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:5476351..5518235hg38UCSC Ensembl
chr20:5456997..5498881hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3841885
hg1941885
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18070205
Samples
Known GenesLINC00654, LOC643406
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522705
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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