A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17003062



Internal ID69663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:104968255..104969130hg38UCSC Ensembl
chr7:104608702..104609577hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38876
hg19876
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5492357
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17003062
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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