A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598590



Internal ID20971661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:5608805..5609301hg38UCSC Ensembl
chr19:5608816..5609312hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38497
hg19497
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248501
Samples
Known GenesSAFB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598590
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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