A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867599



Internal ID22642534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36250840..36254905hg38UCSC Ensembl
chr19:36741742..36745807hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg384066
hg194066
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475271
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867599
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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