A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576288



Internal ID20949359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:48761498..48762072hg38UCSC Ensembl
chr12:49155281..49155855hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg38575
hg19575
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224850
Samples
Known GenesLINC00935
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576288
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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