A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5466174



Internal ID244020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:160196485..160302562hg38UCSC Ensembl
chr4:161117637..161223714hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38106078
hg19106078
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16958991
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5466174
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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