A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552693



Internal ID20925819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:48768656..48769327hg38UCSC Ensembl
chr3:48806089..48806760hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38672
hg19672
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262159
Samples
Known GenesPRKAR2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552693
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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