A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549787



Internal ID20922942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:200990886..200991319hg38UCSC Ensembl
chr2:201855609..201856042hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg38434
hg19434
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256366
Samples
Known GenesFAM126B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549787
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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