A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223795



Internal ID20790835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25162937..25164064hg38UCSC Ensembl
chr10:25451866..25452993hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg381128
hg191128
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6583116
Supporting Variants
Samples
Known GenesGPR158-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223795
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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