A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541559



Internal ID20914841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:64221267..64222025hg38UCSC Ensembl
chr1:64686950..64687708hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38759
hg19759
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv216n223
Supporting Variantsnssv18250611
Samples
Known GenesUBE2U
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541559
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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