A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546559



Internal ID20919769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:157512609..157513428hg38UCSC Ensembl
chr1:157482399..157483218hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg38820
hg19820
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247764
Samples
Known GenesFCRL5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546559
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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