A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5996856



Internal ID21906199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:190122462..190122569hg38UCSC Ensembl
chr4:191043617..191043724hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17547384
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5996856
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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