A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581141



Internal ID20954212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:100298655..100299179hg38UCSC Ensembl
chr12:100692433..100692957hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg38525
hg19525
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218144
Samples
Known GenesSCYL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581141
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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