A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17039786



Internal ID94246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97733744..97745369hg38UCSC Ensembl
chr10:99493501..99505126hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3811626
hg1911626
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563842
Supporting Variants
Samples
Known GenesZFYVE27
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17039786
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.010306


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