A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110206



Internal ID22019439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149968780..150012350hg38UCSC Ensembl
chr6:150289916..150333486hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3843571
hg1943571
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17577346
Samples
Known GenesRAET1K, ULBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110206
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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