A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554776



Internal ID20927867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:153562234..153562881hg38UCSC Ensembl
chr1:153534710..153535357hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38648
hg19648
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247049
Samples
Known GenesS100A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554776
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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