A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363420



Internal ID21020973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:75311001..75525400hg38UCSC Ensembl
chr3:75360152..75574551hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38214400
hg19214400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4912n223
Supporting Variantsnssv18208733
Samples
Known GenesFAM86DP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363420
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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