A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5980202



Internal ID22755137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128530143..128536681hg38UCSC Ensembl
chr11:128400038..128406576hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg386539
hg196539
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17351388
Samples
Known GenesETS1
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5980202
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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