A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232642



Internal ID20799682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:103586872..104687274hg38UCSC Ensembl
chr11:103457600..104558002hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg381100403
hg191100403
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579424
Supporting Variants
Samples
Known GenesDDI1, MIR4693, PDGFD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232642
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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