A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841720



Internal ID22616655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:146199250..146203490hg38UCSC Ensembl
chr5:145578813..145583053hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg384241
hg194241
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17496239
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841720
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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