A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546098



Internal ID20919317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72865398..72866124hg38UCSC Ensembl
chr3:72914549..72915275hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38727
hg19727
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262918
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546098
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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