A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18247767



Internal ID20814807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:157692220..157693146hg38UCSC Ensembl
chr1:157662010..157662936hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg38927
hg19927
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6555271
Supporting Variants
Samples
Known GenesFCRL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18247767
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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