A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879113



Internal ID22654081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:11587929..11596461hg38UCSC Ensembl
chrUn_gl000231:2001..10472hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg388533
hg198472
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17489016, nssv17489015
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879113
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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