A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5466179



Internal ID244025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:181385152..181390793hg38UCSC Ensembl
chr4:182306305..182311946hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg385642
hg195642
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16959637
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5466179
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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