A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17004581



Internal ID70686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:145479199..145529444hg38UCSC Ensembl
chr7:145176292..145226537hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3850246
hg1950246
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5482126
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17004581
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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