A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549659



Internal ID20922820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:102221432..102268258hg38UCSC Ensembl
chr3:101940276..101987102hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg3846827
hg1946827
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259020
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549659
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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