A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18255725



Internal ID20822765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:101087644..101088310hg38UCSC Ensembl
chr2:101704106..101704772hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38667
hg19667
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6549889
Supporting Variants
Samples
Known GenesTBC1D8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18255725
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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