A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559712



Internal ID20932783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:182506208..182506579hg38UCSC Ensembl
chr3:182223996..182224367hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38372
hg19372
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261825
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559712
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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