A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905843



Internal ID22681036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:40334223..40351921hg38UCSC Ensembl
chr5:40334325..40352023hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3817699
hg1917699
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17416689
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5905843
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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