A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596108



Internal ID20969179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:21176581..21177694hg38UCSC Ensembl
chr19:21359384..21360497hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg381114
hg191114
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18246251
Samples
Known GenesZNF431
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596108
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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