A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5839277



Internal ID22614212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3763524..3786445hg38UCSC Ensembl
chr4:3765251..3788172hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3822922
hg1922922
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17494478
Samples
Known GenesADRA2C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5839277
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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