A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5458209



Internal ID236239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2981847..2984098hg38UCSC Ensembl
chr7:3021481..3023732hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg382252
hg192252
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16992379
Samples
Known GenesCARD11
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5458209
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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