A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873052



Internal ID22647995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:30833618..30842254hg38UCSC Ensembl
chr19:31324525..31333161hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg388637
hg198637
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474672
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873052
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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