A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5885179



Internal ID22660164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:30837343..30838342hg38UCSC Ensembl
chr19:31328250..31329249hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474673, nssv17474674
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5885179
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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