A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553047



Internal ID20926162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:60238854..60250407hg38UCSC Ensembl
chr20:58813912..58825465hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3811554
hg1911554
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18069198
Samples
Known GenesLOC284757
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553047
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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