A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599687



Internal ID20972758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:21574057..22827414hg38UCSC Ensembl
chr19:21756859..23010216hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg381253358
hg191253358
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3480n223
Supporting Variantsnssv18244894
Samples
Known GenesLOC100996349, LOC440518, LOC641367, ZNF100, ZNF208, ZNF257, ZNF43, ZNF492, ZNF676, ZNF729, ZNF98, ZNF99
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599687
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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