A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541191



Internal ID20914475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:186637402..189474697hg38UCSC Ensembl
chr1:186606534..189443827hg19UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg382837296
hg192837294
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv463n223
Supporting Variantsnssv18249551
Samples
Known GenesPLA2G4A, PTGS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541191
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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