A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5842959



Internal ID22617894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:33393066..33429049hg38UCSC Ensembl
chr5:33393172..33429155hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3835984
hg1935984
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17496607
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5842959
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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