A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578778



Internal ID20951849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110608291..110609117hg38UCSC Ensembl
chr12:111046096..111046922hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38827
hg19827
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226670
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578778
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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