A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369279



Internal ID21026832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:52459508..52467133hg38UCSC Ensembl
chr3:52493524..52501149hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg387626
hg197626
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209987
Samples
Known GenesNISCH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369279
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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