A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538588



Internal ID20911901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:226774125..226774738hg38UCSC Ensembl
chr1:226961826..226962439hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg38614
hg19614
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250290
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538588
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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