A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5872391



Internal ID22647331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10667375..10668524hg38UCSC Ensembl
chr19:10778051..10779200hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381150
hg191150
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17472635, nssv17472634
Samples
Known GenesILF3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5872391
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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