A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5963666



Internal ID22738601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:57767380..57767439hg38UCSC Ensembl
chr20:56342436..56342495hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17392262
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5963666
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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