A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6147283



Internal ID346465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18246662..18268073hg38UCSC Ensembl
chr11:18268209..18289620hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3821412
hg1921412
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv67n206
Supporting Variantsnssv17043686
Samples
Known GenesSAA1, SAA2, SAA2-SAA4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6147283
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer