A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871191



Internal ID22646128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:18079172..18081275hg38UCSC Ensembl
chr19:18189982..18192085hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg382104
hg192104
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473329
Samples
Known GenesIL12RB1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871191
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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