A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544021



Internal ID20917262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109577279..109578343hg38UCSC Ensembl
chr1:110119901..110120965hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg381065
hg191065
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv303n223
Supporting Variantsnssv18247304
Samples
Known GenesGNAI3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544021
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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