A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553988



Internal ID20927097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:243430456..243430972hg38UCSC Ensembl
chr1:243593758..243594274hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg38517
hg19517
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250187
Samples
Known GenesSDCCAG8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553988
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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