A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224795



Internal ID20791835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103189000..103190018hg38UCSC Ensembl
chr10:104948757..104949775hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg381019
hg191019
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581711
Supporting Variants
Samples
Known GenesNT5C2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224795
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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