A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546698



Internal ID20919908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:202328536..202329868hg38UCSC Ensembl
chr2:203193259..203194591hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg381333
hg191333
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257712
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546698
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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