A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233196



Internal ID20800236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100265085..100265284hg38UCSC Ensembl
chr10:102024842..102025041hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg38200
hg19200
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6593415
Supporting Variants
Samples
Known GenesCWF19L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233196
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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