A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599208



Internal ID20972279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45868494..45869027hg38UCSC Ensembl
chr19:46371752..46372285hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38534
hg19534
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245662
Samples
Known GenesFOXA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599208
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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