A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875586



Internal ID22650544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:30988403..30993741hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg385339
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1322n209
Supporting Variantsnssv17485225, nssv17485226
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875586
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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