A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361929



Internal ID21019482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:142511569..142512031hg38UCSC Ensembl
chr3:142230411..142230873hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38463
hg19463
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209665
Samples
Known GenesATR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361929
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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