A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218929



Internal ID20785969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32631169..32631263hg38UCSC Ensembl
chr11:32652715..32652809hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6583762
Supporting Variants
Samples
Known GenesCCDC73
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218929
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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