A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5885142



Internal ID22660126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:45988971..45998324hg38UCSC Ensembl
chr20:44617610..44626963hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg389354
hg199354
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17486060
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5885142
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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