A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551132



Internal ID20924272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:234363955..234365262hg38UCSC Ensembl
chr1:234499701..234501008hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg381308
hg191308
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250668
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551132
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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