A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217151



Internal ID20784191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112038405..112039002hg38UCSC Ensembl
chr10:113798163..113798760hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38598
hg19598
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6578415
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217151
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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