A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17584399



Internal ID21776442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1660904..1683270hg38UCSC Ensembl
chr11:1682134..1704500hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3822367
hg1922367
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6103716
Supporting Variants
Samples
Known GenesFAM99A, MOB2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17584399
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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