A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871613



Internal ID22646551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8101627..8103328hg38UCSC Ensembl
chr19:8166511..8168212hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381702
hg191702
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17480402
Samples
Known GenesFBN3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871613
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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