A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5842120



Internal ID22617055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:170762299..170767124hg38UCSC Ensembl
chr5:170189303..170194128hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg384826
hg194826
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17497686
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5842120
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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