A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905185



Internal ID22680369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:173680133..173680199hg38UCSC Ensembl
chr5:173107136..173107202hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17427920
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5905185
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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