A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5872880



Internal ID22647822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:3494305..3497699hg38UCSC Ensembl
chr20:3474952..3478346hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg383395
hg193395
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485328
Samples
Known GenesATRN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5872880
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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