A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880388



Internal ID22655358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29440163..29441916hg38UCSC Ensembl
chr19:29931070..29932823hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg381754
hg191754
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474650
Samples
Known GenesLOC284395
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880388
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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