A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18257706



Internal ID20824746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:202288809..202289924hg38UCSC Ensembl
chr2:203153532..203154647hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg381116
hg191116
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6548302
Supporting Variants
Samples
Known GenesNOP58
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18257706
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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