A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555039



Internal ID20928128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:200993890..200994434hg38UCSC Ensembl
chr2:201858613..201859157hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg38545
hg19545
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256367
Samples
Known GenesFAM126B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555039
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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