A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598886



Internal ID20971957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2851018..2852126hg38UCSC Ensembl
chr19:2851016..2852124hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381109
hg191109
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245846
Samples
Known GenesZNF555
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598886
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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