A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17688945



Internal ID112611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:70728154..70728330hg38UCSC Ensembl
chr12:71121934..71122110hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560176
Supporting Variants
Samples
Known GenesPTPRR
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17688945
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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