A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356690



Internal ID21014243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:106000199..106007022hg38UCSC Ensembl
chr3:105719046..105725869hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg386824
hg196824
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093703
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356690
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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