A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841542



Internal ID22616477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:161712919..161715341hg38UCSC Ensembl
chr5:161139925..161142347hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg382423
hg192423
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1721n209
Supporting Variantsnssv17496996
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841542
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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