A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220154



Internal ID20787194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4679223..4680559hg38UCSC Ensembl
chr10:4721415..4722751hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg381337
hg191337
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579461
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220154
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0027


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