A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369010



Internal ID21026563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:35029001..35056100hg38UCSC Ensembl
chr4:35030623..35057722hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3827100
hg1927100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5228n223
Supporting Variantsnssv18213522
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369010
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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