A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554364



Internal ID20927466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:154362886..154395496hg38UCSC Ensembl
chr1:154335362..154367972hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3832611
hg1932611
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv392n223
Supporting Variantsnssv18247089
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554364
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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