A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401388



Internal ID21058941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:79076801..79079100hg38UCSC Ensembl
chr6:79786518..79788817hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6286n223
Supporting Variantsnssv18228724
Samples
Known GenesPHIP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401388
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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