A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5842198



Internal ID22617133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:174418572..174420552hg38UCSC Ensembl
chr5:173845575..173847555hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg381981
hg191981
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17497727
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5842198
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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