A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871098



Internal ID22646036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:53664661..53666425hg38UCSC Ensembl
chr19:54167915..54169679hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg381765
hg191765
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17478039
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871098
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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