A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6353286



Internal ID21010839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:241844201..242006600hg38UCSC Ensembl
chr2:242786353..242948751hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38162400
hg19162399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4328n223
Supporting Variantsnssv18209032
Samples
Known GenesCXXC11, PDCD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6353286
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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