A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5902158



Internal ID22677313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:161711732..161715641hg38UCSC Ensembl
chr5:161138738..161142647hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg383910
hg193910
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17427451
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5902158
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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