A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892780



Internal ID22667835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:145381459..145407528hg38UCSC Ensembl
chr5:144761022..144787091hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3826070
hg1926070
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17415090
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892780
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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