A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406804



Internal ID21064357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6961901..6966292hg38UCSC Ensembl
chr6:6962134..6966525hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg384392
hg194392
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233684
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406804
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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