A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577373



Internal ID20950444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:47279735..47280298hg38UCSC Ensembl
chr12:47673518..47674081hg19UCSC Ensembl
Cytoband12q13.11
Allele length
AssemblyAllele length
hg38564
hg19564
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218922
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577373
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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