A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18248138



Internal ID20815178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151211862..151212652hg38UCSC Ensembl
chr1:151184338..151185128hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38791
hg19791
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6546483
Supporting Variants
Samples
Known GenesPIP5K1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18248138
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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