A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18248024



Internal ID20815064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:167051244..167052984hg38UCSC Ensembl
chr1:167020481..167022221hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg381741
hg191741
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540345
Supporting Variants
Samples
Known GenesGPA33
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18248024
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00015


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