A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370394



Internal ID21027947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:105110255..105347140hg38UCSC Ensembl
chr3:104829099..105065984hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38236886
hg19236886
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093044
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370394
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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