A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596228



Internal ID20969299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11975156..11976419hg38UCSC Ensembl
chr19:12085971..12087234hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381264
hg191264
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3441n223
Supporting Variantsnssv18245035
Samples
Known GenesZNF763
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596228
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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