A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6379667



Internal ID21037220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:10119279..10178200hg38UCSC Ensembl
chr5:10119391..10178312hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3858922
hg1958922
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214456
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6379667
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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