A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874624



Internal ID22649578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34849044..34851593hg38UCSC Ensembl
chr19:35339948..35342497hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg382550
hg192550
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475244
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874624
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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