A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599518



Internal ID20972589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11975380..11978339hg38UCSC Ensembl
chr19:12086195..12089154hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg382960
hg192960
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245036
Samples
Known GenesZNF763
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599518
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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