A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17406889



Internal ID22464759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63026408..63026700hg38UCSC Ensembl
chr20:61657760..61658052hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38293
hg19293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5951728
Supporting Variants
Samples
Known GenesLOC63930
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17406889
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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