A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5898016



Internal ID22673127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:139489640..139489690hg38UCSC Ensembl
chr5:138869225..138869275hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17418489
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5898016
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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