A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969095



Internal ID22744030
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 StatusM
Merged Variants
Supporting Variantsnssv17421379
Samples
Known GenesRAET1K, RAET1L, ULBP1, ULBP2
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969095
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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