A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6358845



Internal ID21016398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:43861465..43861714hg38UCSC Ensembl
chr3:43902957..43903206hg19UCSC Ensembl
Cytoband3p21.33
Allele length
AssemblyAllele length
hg38250
hg19250
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099981
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6358845
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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