A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5462246



Internal ID240177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:140076385..140188743hg38UCSC Ensembl
chr6:140397522..140509880hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38112359
hg19112359
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16970226
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5462246
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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