A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368460



Internal ID21026013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16408578..16408845hg38UCSC Ensembl
chr3:16450085..16450352hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18095490
Samples
Known GenesRFTN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368460
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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