A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6147180



Internal ID346362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:16910430..16973414hg38UCSC Ensembl
chr17:16813744..16876728hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3862985
hg1962985
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17711828
Samples
Known GenesTNFRSF13B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6147180
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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