A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5949997



Internal ID22725437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:64055420..64055477hg38UCSC Ensembl
chr20:62686773..62686830hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17404279
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5949997
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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