A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5455519



Internal ID233598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:21826133..21826338hg38UCSC Ensembl
chr7:21865751..21865956hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16992918
Samples
Known GenesDNAH11
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5455519
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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