A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5468352



Internal ID246150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:71472304..71472372hg38UCSC Ensembl
chr6:72182007..72182075hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16987186
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5468352
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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