A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596150



Internal ID20969221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:18351585..18352974hg38UCSC Ensembl
chr19:18462395..18463784hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg381390
hg191390
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247602
Samples
Known GenesPGPEP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596150
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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