A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6402119



Internal ID21059672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:22166401..22171300hg38UCSC Ensembl
chr6:22166630..22171529hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg384900
hg194900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6087n223
Supporting Variantsnssv18218277
Samples
Known GenesCASC15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6402119
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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