A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219015



Internal ID20786055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32678633..32679413hg38UCSC Ensembl
chr11:32700179..32700959hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38781
hg19781
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6593909
Supporting Variants
Samples
Known GenesCCDC73
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219015
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00026


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