A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841530



Internal ID22616465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:157866467..157875916hg38UCSC Ensembl
chr5:157293475..157302924hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg389450
hg199450
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17496930, nssv17496931
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841530
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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