A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554110



Internal ID20927219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:185994052..187137812hg38UCSC Ensembl
chr1:185963184..187106944hg19UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg381143761
hg191143761
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249544
Samples
Known GenesC1orf27, HMCN1, MIR548F1, OCLM, PDC, PLA2G4A, PRG4, PTGS2, RNU6-72P, TPR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554110
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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