A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598401



Internal ID20971472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16488170..16489270hg38UCSC Ensembl
chr19:16598981..16600081hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg381101
hg191101
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247555
Samples
Known GenesCALR3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598401
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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