A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17709955



Internal ID133621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:1501958..1584136hg38UCSC Ensembl
chr17:1405252..1487430hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3882179
hg1982179
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557915
Supporting Variants
Samples
Known GenesINPP5K, PITPNA, PITPNA-AS1, SLC43A2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17709955
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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