A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5842111



Internal ID22617046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:167173281..167182779hg38UCSC Ensembl
chr5:166600286..166609784hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg389499
hg199499
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17497080
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5842111
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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