A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16992850



Internal ID62699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:20758724..20765015hg38UCSC Ensembl
chr7:20798347..20804638hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg386292
hg196292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5454951
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16992850
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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