A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231846



Internal ID20798886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100111005..100111659hg38UCSC Ensembl
chr10:101870762..101871416hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38655
hg19655
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582177
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231846
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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