A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538044



Internal ID20911370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:60234101..60235800hg38UCSC Ensembl
chr20:58809159..58810858hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18069197
Samples
Known GenesLOC284757
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538044
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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