A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5464205



Internal ID242086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:133852913..133863747hg38UCSC Ensembl
chr5:133188604..133199438hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3810835
hg1910835
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16973954
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5464205
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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