A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905676



Internal ID22680866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:100065175..100379307hg38UCSC Ensembl
chr5:99400879..99715011hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg38314133
hg19314133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424482
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5905676
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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