A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970839



Internal ID22745774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:74527352..75035369hg38UCSC Ensembl
chr11:74238397..74746414hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38508018
hg19508018
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17356162
Samples
Known GenesCHRDL2, MIR4696, NEU3, POLD3, RNF169, SPCS2, XRRA1
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970839
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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