A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905367



Internal ID22680553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:161907341..161908950hg38UCSC Ensembl
chr5:161334347..161335956hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg381610
hg191610
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17425165
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5905367
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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