A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369878



Internal ID21027431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:6657975..6668797hg38UCSC Ensembl
chr3:6699662..6710484hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3810823
hg1910823
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18102258
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369878
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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