A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5869782



Internal ID22644717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56695691..56700919hg38UCSC Ensembl
chr20:55270747..55275975hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg385229
hg195229
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17486711
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5869782
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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