A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841926



Internal ID22616861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:178488949..178538420hg38UCSC Ensembl
chr5:177915950..177965421hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3849472
hg1949472
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17495000, nssv17498408
Samples
Known GenesCOL23A1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841926
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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