A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560969



Internal ID333960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149968869..150001337hg38UCSC Ensembl
chr6:150290005..150322473hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3832469
hg1932469
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv433n206
Supporting Variantsnssv16989654
Samples
Known GenesRAET1K, ULBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560969
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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