A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555271



Internal ID20928362
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 StatusM
Merged Variants
Supporting Variantsnssv18247767
Samples
Known GenesFCRL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555271
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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