A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595310



Internal ID20968381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:25425961..25427036hg38UCSC Ensembl
chr12:25578895..25579970hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg381076
hg191076
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228445
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595310
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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