A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5556919



Internal ID330038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:96399529..96399878hg38UCSC Ensembl
chr11:96132693..96133042hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38350
hg19350
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17052141
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5556919
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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