A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579192



Internal ID20952263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:76396519..76396939hg38UCSC Ensembl
chr12:76790299..76790719hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg38421
hg19421
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1618n223
Supporting Variantsnssv18235436
Samples
Known GenesOSBPL8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579192
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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