A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18259364



Internal ID20826404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:219134812..219136729hg38UCSC Ensembl
chr2:219999534..220001451hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg381918
hg191918
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6542783
Supporting Variants
Samples
Known GenesNHEJ1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18259364
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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