A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6344412



Internal ID21001965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:165636301..165653584hg38UCSC Ensembl
chr2:166492811..166510094hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3817284
hg1917284
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207349
Samples
Known GenesCSRNP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6344412
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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