A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6353010



Internal ID21010563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:228532498..228568663hg38UCSC Ensembl
chr2:229397214..229433379hg19UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg3836166
hg1936166
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206158
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6353010
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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