A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5901926



Internal ID22677079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:157242425..157243006hg38UCSC Ensembl
chr5:156669435..156670016hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg38582
hg19582
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17416886
Samples
Known GenesITK
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5901926
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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