A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892704



Internal ID22667758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:159766491..159766703hg38UCSC Ensembl
chr5:159193498..159193710hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg38213
hg19213
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17426373
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892704
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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