A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555082



Internal ID20928171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:33139126..33139646hg38UCSC Ensembl
chr3:33180618..33181138hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38521
hg19521
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262029
Samples
Known GenesCRTAP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555082
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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