A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5464264



Internal ID242145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:98167571..98186711hg38UCSC Ensembl
chr6:98615447..98634587hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3819141
hg1919141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16985226
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5464264
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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