A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5671123



Internal ID21619428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65500258..65505993hg38UCSC Ensembl
chr11:65267729..65273464hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg385736
hg195736
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17075277
SamplesNA19240
Known GenesMALAT1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5671123
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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