A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6337550



Internal ID20995103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:142366182..142387965hg38UCSC Ensembl
chr2:143123751..143145534hg19UCSC Ensembl
Cytoband2q22.2
Allele length
AssemblyAllele length
hg3821784
hg1921784
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207263
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6337550
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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