A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841382



Internal ID22616317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:122584093..122585692hg38UCSC Ensembl
chr5:121919788..121921387hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17493884
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841382
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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