A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367868



Internal ID21025421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:147753901..147754800hg38UCSC Ensembl
chr3:147471688..147472587hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5050n223
Supporting Variantsnssv18095762
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367868
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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