A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219084



Internal ID20786124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112887691..112888670hg38UCSC Ensembl
chr10:114647450..114648429hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38980
hg19980
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6592012
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219084
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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