A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219122



Internal ID20786162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21101301..21108755hg38UCSC Ensembl
chr10:21390230..21397684hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg387455
hg197455
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6593511
Supporting Variants
Samples
Known GenesNEBL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219122
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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