A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577462



Internal ID20950533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:66057681..66281138hg38UCSC Ensembl
chr12:66451461..66674918hg19UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg38223458
hg19223458
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223885
Samples
Known GenesIRAK3, LLPH, TMBIM4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577462
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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