A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897941



Internal ID22673051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:113798628..113859891hg38UCSC Ensembl
chr5:113134325..113195588hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3861264
hg1961264
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17417453
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5897941
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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