A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537531



Internal ID20910866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:207717976..207718496hg38UCSC Ensembl
chr2:208582700..208583220hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg38521
hg19521
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258563
Samples
Known GenesCCNYL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537531
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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