A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873063



Internal ID22648006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:16290682..16295981hg38UCSC Ensembl
chr21:17663003..17668302hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg385300
hg195300
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17487985
Samples
Known GenesLINC00478
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873063
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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