A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17365682



Internal ID22591351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94121081..94123712hg38UCSC Ensembl
chr11:93854247..93856878hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg382632
hg192632
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5972110
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17365682
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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