A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360341



Internal ID21017894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:52992001..53045200hg38UCSC Ensembl
chr3:53026017..53079216hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg3853200
hg1953200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4874n223
Supporting Variantsnssv18210002
Samples
Known GenesSFMBT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360341
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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