A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597966



Internal ID20971037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4846119..4847086hg38UCSC Ensembl
chr19:4846131..4847098hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38968
hg19968
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18246388
Samples
Known GenesPLIN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597966
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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