A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359593



Internal ID21017146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:182461799..182479142hg38UCSC Ensembl
chr3:182179587..182196930hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg3817344
hg1917344
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18097868
Samples
Known GenesFLJ46066
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359593
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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