A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17000845



Internal ID68131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:104131837..104134349hg38UCSC Ensembl
chr7:103772284..103774796hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg382513
hg192513
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5489881
Supporting Variants
Samples
Known GenesORC5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17000845
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001405


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