A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868102



Internal ID22643037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:11593880..11595960hg38UCSC Ensembl
chrUn_gl000231:7891..9971hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg382081
hg192081
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17481020, nssv17481019
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868102
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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