A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905690



Internal ID22680880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:153324475..153338069hg38UCSC Ensembl
chr5:152704035..152717629hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg3813595
hg1913595
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424165
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5905690
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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