A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6147192



Internal ID346374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35699212..35707498hg38UCSC Ensembl
chr11:35720760..35729046hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg388287
hg198287
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17044248
Samples
Known GenesTRIM44
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6147192
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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