A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553093



Internal ID20926208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72953862..72954078hg38UCSC Ensembl
chr3:73003013..73003229hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38217
hg19217
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262922
Samples
Known GenesGXYLT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553093
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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