A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18247519



Internal ID20814559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150350075..150351173hg38UCSC Ensembl
chr1:150322551..150323649hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg381099
hg191099
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6553051
Supporting Variants
Samples
Known GenesPRPF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18247519
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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