A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538599



Internal ID20911912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:92954711..92955513hg38UCSC Ensembl
chr1:93420268..93421070hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg38803
hg19803
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv270n223
Supporting Variantsnssv18252729
Samples
Known GenesFAM69A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538599
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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