A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598191



Internal ID20971262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38828790..38829101hg38UCSC Ensembl
chr19:39319430..39319741hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248380
Samples
Known GenesECH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598191
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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