A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5953601



Internal ID22728880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:19162497..19187953hg38UCSC Ensembl
chr20:19143141..19168597hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg3825457
hg1925457
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17392590
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5953601
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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