A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876367



Internal ID22651328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:21793850..21818262hg38UCSC Ensembl
chr1:22120343..22144755hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3824413
hg1924413
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17366694
Samples
Known GenesLDLRAD2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876367
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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