A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363869



Internal ID21021422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:170901095..170902194hg38UCSC Ensembl
chr3:170618884..170619983hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18097180
Samples
Known GenesEIF5A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363869
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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