A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365204



Internal ID21022757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4048553..4211199hg38UCSC Ensembl
chr3:4090237..4252883hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38162647
hg19162647
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4765n223
Supporting Variantsnssv18099144
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365204
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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