A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5977403



Internal ID22752338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9983770..9985585hg38UCSC Ensembl
chr11:10005317..10007132hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381816
hg191816
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17366501
Samples
Known GenesSBF2
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5977403
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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