A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5455536



Internal ID233614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108096451..108098557hg38UCSC Ensembl
chr6:108417655..108419761hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg382107
hg192107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16986699
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5455536
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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