A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6414696



Internal ID21072249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:22165001..22192000hg38UCSC Ensembl
chr6:22165230..22192229hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3827000
hg1927000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6086n223
Supporting Variantsnssv18224399
Samples
Known GenesCASC15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6414696
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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