A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17000364



Internal ID67827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:92473622..92476320hg38UCSC Ensembl
chr7:92102936..92105634hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg382699
hg192699
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5492647
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17000364
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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