A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360375



Internal ID21017928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:35761701..35897500hg38UCSC Ensembl
chr3:35803193..35938992hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38135800
hg19135800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4843n223
Supporting Variantsnssv18211156
Samples
Known GenesARPP21
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360375
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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