A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16991955



Internal ID62084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:5779796..5780662hg38UCSC Ensembl
chr7:5819427..5820293hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38867
hg19867
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5453956
Supporting Variants
Samples
Known GenesRNF216
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16991955
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001093


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