A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841726



Internal ID22616661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:147800294..147801693hg38UCSC Ensembl
chr5:147179857..147181256hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17496261, nssv17496262
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841726
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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