A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5455834



Internal ID233906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:16848691..16954976hg38UCSC Ensembl
chr7:16888315..16994600hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38106286
hg19106286
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16993850
Samples
Known GenesAGR3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5455834
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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