A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5885816



Internal ID22660802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:31578073..31591385hg38UCSC Ensembl
chr20:30165876..30179188hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3813313
hg1913313
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485272
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5885816
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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