A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18246694



Internal ID20813734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:52277471..52277994hg38UCSC Ensembl
chr19:52780724..52781247hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38524
hg19524
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6598172
Supporting Variants
Samples
Known GenesZNF766
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18246694
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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