A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369120



Internal ID21026673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:35761601..35902800hg38UCSC Ensembl
chr3:35803093..35944292hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38141200
hg19141200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4843n223
Supporting Variantsnssv18210564
Samples
Known GenesARPP21
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369120
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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