A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968960



Internal ID22743895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1665569..1685706hg38UCSC Ensembl
chr11:1686799..1706936hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3820138
hg1920138
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17361290
Samples
Known GenesFAM99A, FAM99B, MOB2
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968960
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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