A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366711



Internal ID21024264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:35761501..35804200hg38UCSC Ensembl
chr3:35802993..35845692hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3842700
hg1942700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4844n223
Supporting Variantsnssv18210563
Samples
Known GenesARPP21
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366711
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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