A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221257



Internal ID20788297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:104554685..109812699hg38UCSC Ensembl
chr10:106314443..111572457hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg385258015
hg195258015
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6594084
Supporting Variants
Samples
Known GenesRNU6-53P, SORCS1, SORCS3, SORCS3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221257
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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