A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18245037



Internal ID20812077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11975534..11976547hg38UCSC Ensembl
chr19:12086349..12087362hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381014
hg191014
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6598443
Supporting Variants
Samples
Known GenesZNF763
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18245037
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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