A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549655



Internal ID20922816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:48778667..48779626hg38UCSC Ensembl
chr3:48816100..48817059hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38960
hg19960
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262161
Samples
Known GenesPRKAR2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549655
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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