A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5473749



Internal ID251432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:112317928..112318569hg38UCSC Ensembl
chr6:112639130..112639771hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38642
hg19642
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16986464
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5473749
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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