A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5461256



Internal ID239216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:43197208..43197645hg38UCSC Ensembl
chr6:43164946..43165383hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38438
hg19438
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16981664
Samples
Known GenesCUL9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5461256
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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