A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18255402



Internal ID20822442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:169660219..169660735hg38UCSC Ensembl
chr2:170516729..170517245hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38517
hg19517
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6542944
Supporting Variants
Samples
Known GenesCCDC173
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18255402
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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