A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5840319



Internal ID22615254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:105931085..105932284hg38UCSC Ensembl
chr5:105266786..105267985hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17492390
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5840319
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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