A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16989653



Internal ID60525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149965959..150004309hg38UCSC Ensembl
chr6:150287095..150325445hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3838351
hg1938351
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6147010
Supporting Variants
Samples
Known GenesRAET1K, ULBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16989653
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.001562


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