A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841841



Internal ID22616776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:162634059..162642625hg38UCSC Ensembl
chr5:162061065..162069631hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg388567
hg198567
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17497010
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841841
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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