A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544992



Internal ID20918229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50273053..50281306hg38UCSC Ensembl
chr20:48889590..48897843hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg388254
hg198254
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18069057
Samples
Known GenesLOC100506115
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544992
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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