A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554834



Internal ID20927924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:184765150..184765634hg38UCSC Ensembl
chr1:184734284..184734768hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg38485
hg19485
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249527
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554834
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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