A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585833



Internal ID20958904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:68778836..68780288hg38UCSC Ensembl
chr12:69172616..69174068hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg381453
hg191453
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219729
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585833
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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