A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571859



Internal ID20944930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:182522892..182524350hg38UCSC Ensembl
chr3:182240680..182242138hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg381459
hg191459
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261826
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571859
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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