A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5455960



Internal ID234028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:85236287..85240757hg38UCSC Ensembl
chr6:85946005..85950475hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg384471
hg194471
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16984327
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5455960
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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