A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6344957



Internal ID21002510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:225833659..226053634hg38UCSC Ensembl
chr2:226698375..226918350hg19UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg38219976
hg19219976
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206108
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6344957
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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