A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18262169



Internal ID20829209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:48831634..48832177hg38UCSC Ensembl
chr3:48869067..48869610hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38544
hg19544
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6545260
Supporting Variants
Samples
Known GenesPRKAR2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18262169
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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