A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232171



Internal ID20799211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:17131102..17131533hg38UCSC Ensembl
chr11:17152649..17153080hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38432
hg19432
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6586597
Supporting Variants
Samples
Known GenesPIK3C2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232171
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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