A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596976



Internal ID20970047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17978446..17979160hg38UCSC Ensembl
chr19:18089255..18089969hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38715
hg19715
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247592
Samples
Known GenesKCNN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596976
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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