A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18068581



Internal ID20635621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63101628..63123641hg38UCSC Ensembl
chr20:61732980..61754993hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3822014
hg1922014
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6554589
Supporting Variants
Samples
Known GenesHAR1A, HAR1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18068581
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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