A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18256190



Internal ID20823231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:176467892..176469507hg38UCSC Ensembl
chr2:177332620..177334235hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg381616
hg191616
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6553683
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18256190
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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