A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17000609



Internal ID67986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:105332129..105529172hg38UCSC Ensembl
chr7:104972576..105169619hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38197044
hg19197044
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560079
Supporting Variants
Samples
Known GenesPUS7, SRPK2
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17000609
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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