A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377068



Internal ID21034621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:3186101..3196100hg38UCSC Ensembl
chr5:3186215..3196214hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3810000
hg1910000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216180
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377068
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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