A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584921



Internal ID20957992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:24257673..24258194hg38UCSC Ensembl
chr12:24410607..24411128hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38522
hg19522
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1445n223
Supporting Variantsnssv18217341
Samples
Known GenesSOX5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584921
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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