A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5997808



Internal ID21907151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:66711953..66712110hg38UCSC Ensembl
chr4:67577671..67577828hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38158
hg19158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17547067
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5997808
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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