A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588086



Internal ID20961157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:24882853..24883027hg38UCSC Ensembl
chr12:25035787..25035961hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38175
hg19175
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235670
Samples
Known GenesBCAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588086
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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