A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578386



Internal ID20951457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:121596830..121598158hg38UCSC Ensembl
chr12:122034735..122036063hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg381329
hg191329
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218476
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578386
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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