A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592888



Internal ID20965959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:78498247..78510984hg38UCSC Ensembl
chr12:78892027..78904764hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg3812738
hg1912738
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217336
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592888
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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