A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594467



Internal ID20967538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:40132474..40134022hg38UCSC Ensembl
chr12:40526276..40527824hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg381549
hg191549
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228826
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594467
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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