A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224529



Internal ID20791569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:63338656..63340071hg38UCSC Ensembl
chr10:65098416..65099831hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg381416
hg191416
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579623
Supporting Variants
Samples
Known GenesJMJD1C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224529
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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