A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553259



Internal ID20926368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32030700..32031759hg38UCSC Ensembl
chr3:32072192..32073251hg19UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg381060
hg191060
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261368
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553259
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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