A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18069172



Internal ID20636212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:59838442..59839078hg38UCSC Ensembl
chr20:58413497..58414133hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38637
hg19637
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6544637
Supporting Variants
Samples
Known GenesPHACTR3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18069172
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00026


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