A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17026110



Internal ID85139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89159094..89159145hg38UCSC Ensembl
chr9:91774009..91774060hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg386016
hg196016
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5562049
Supporting Variants
Samples
Known GenesSHC3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17026110
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.005639


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