A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17002921



Internal ID69563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99853775..99865035hg38UCSC Ensembl
chr7:99451398..99462658hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3811261
hg1911261
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560210
Supporting Variants
Samples
Known GenesCYP3A43
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17002921
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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