A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17421379



Internal ID22479249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149943635..150023033hg38UCSC Ensembl
chr6:150264771..150344169hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3879399
hg1979399
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5969095
Supporting Variants
Samples
Known GenesRAET1K, RAET1L, ULBP1, ULBP2
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17421379
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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