A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363481



Internal ID21021034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:109413741..109416700hg38UCSC Ensembl
chr3:109132588..109135547hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg382960
hg192960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18092483
Samples
Known GenesFLJ25363
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363481
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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