A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5872478



Internal ID22647418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34777637..34781820hg38UCSC Ensembl
chr19:35268542..35272724hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg384184
hg194183
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475242
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5872478
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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