A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897691



Internal ID22672797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:124220333..124220789hg38UCSC Ensembl
chr5:123556026..123556482hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg38457
hg19457
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17415645
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5897691
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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