A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368409



Internal ID21025962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:134538901..134539400hg38UCSC Ensembl
chr3:134257743..134258242hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094833
Samples
Known GenesCEP63
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368409
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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