A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559447



Internal ID20932518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:151279081..151280001hg38UCSC Ensembl
chr4:152200233..152201153hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38921
hg19921
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5522n223
Supporting Variantsnssv18263843
Samples
Known GenesPRSS48
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559447
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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