A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5558289



Internal ID331357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149962199..150071061hg38UCSC Ensembl
chr6:150283335..150392197hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38108863
hg19108863
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16989652
Samples
Known GenesRAET1K, RAET1L, ULBP1, ULBP3
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5558289
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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