A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551491



Internal ID20924625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28097452..28097885hg38UCSC Ensembl
chr1:28423963..28424396hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38434
hg19434
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249643
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551491
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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