A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6348843



Internal ID21006396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:226496512..226577879hg38UCSC Ensembl
chr2:227361228..227442595hg19UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg3881368
hg1981368
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206114
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6348843
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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