A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593769



Internal ID20966840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:41666881..41677792hg38UCSC Ensembl
chr12:42060683..42071594hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg3810912
hg1910912
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217346
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593769
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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