A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357336



Internal ID21014889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:172711020..172721725hg38UCSC Ensembl
chr3:172428810..172439515hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3810706
hg1910706
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209225
Samples
Known GenesNCEH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6357336
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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