A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579437



Internal ID20952508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:111651257..111651995hg38UCSC Ensembl
chr12:112089061..112089799hg19UCSC Ensembl
Cytoband12q24.12
Allele length
AssemblyAllele length
hg38739
hg19739
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222598
Samples
Known GenesBRAP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579437
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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