A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882629



Internal ID22657606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56583847..56585396hg38UCSC Ensembl
chr20:55158903..55160452hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg381550
hg191550
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17486709
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5882629
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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