A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364918



Internal ID21022471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:106887178..107302306hg38UCSC Ensembl
chr3:106606025..107021153hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg38415129
hg19415129
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207197
Samples
Known GenesLINC00882, LINC00883
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364918
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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