A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585998



Internal ID20959069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:20231354..20236987hg38UCSC Ensembl
chr12:20384288..20389921hg19UCSC Ensembl
Cytoband12p12.2
Allele length
AssemblyAllele length
hg385634
hg195634
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231843
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585998
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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