A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367328



Internal ID21024881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:5075133..5093125hg38UCSC Ensembl
chr3:5116818..5134810hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3817993
hg1917993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18102232
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367328
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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