A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363132



Internal ID21020685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98727631..98728385hg38UCSC Ensembl
chr3:98446475..98447229hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg38755
hg19755
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18104945
Samples
Known GenesST3GAL6-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363132
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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