A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907099



Internal ID22682304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169759734..169762746hg38UCSC Ensembl
chr4:170680885..170683897hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg383013
hg193013
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17420219
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907099
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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