A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5461831



Internal ID239774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:117720752..117720802hg38UCSC Ensembl
chr6:118041915..118041965hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16987700
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5461831
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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