A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16993220



Internal ID62931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:22872439..22943440hg38UCSC Ensembl
chr7:22912058..22983059hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3871002
hg1971002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5459143
Supporting Variants
Samples
Known GenesFAM126A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16993220
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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