A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841521



Internal ID22616456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:161589420..161609573hg38UCSC Ensembl
chr5:161016426..161036579hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3820154
hg1920154
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17496993
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841521
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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