A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17000282



Internal ID67772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:108577847..108587856hg38UCSC Ensembl
chr7:108218291..108228300hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3810010
hg1910010
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5484393
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17000282
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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