A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544643



Internal ID20917881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:207746711..207747556hg38UCSC Ensembl
chr2:208611435..208612280hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg38846
hg19846
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258565
Samples
Known GenesCCNYL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544643
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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