A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5971632



Internal ID22746567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:57520314..57522579hg38UCSC Ensembl
chr11:57287787..57290052hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg382266
hg192266
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17364376
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5971632
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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