A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554768



Internal ID20927859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:209889627..209935469hg38UCSC Ensembl
chr1:210062972..210108814hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3845843
hg1945843
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv518n223
Supporting Variantsnssv18247848
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554768
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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