A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16992474



Internal ID62446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:4732658..4732721hg38UCSC Ensembl
chr7:4772289..4772352hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5466431
Supporting Variants
Samples
Known GenesFOXK1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16992474
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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