A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5459969



Internal ID237971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:168754630..168755993hg38UCSC Ensembl
chr4:169675781..169677144hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg381364
hg191364
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16957856
Samples
Known GenesPALLD
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5459969
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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