A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590355



Internal ID20963426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:122410017..122411196hg38UCSC Ensembl
chr12:122894564..122895743hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg381180
hg191180
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221152
Samples
Known GenesCLIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590355
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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