A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540539



Internal ID20913832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:200858158..200933532hg38UCSC Ensembl
chr1:200827286..200902660hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3875375
hg1975375
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248293
Samples
Known GenesC1orf106, CAMSAP2, GPR25
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540539
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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