A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17712482



Internal ID136148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:30470256..30470354hg38UCSC Ensembl
chr17:28797274..28797372hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5558881
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17712482
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000468


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