A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556529



Internal ID20929600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:185553721..185554581hg38UCSC Ensembl
chr3:185271509..185272369hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg38861
hg19861
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5119n223
Supporting Variantsnssv18261218
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556529
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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