A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604778



Internal ID20977849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:109045701..109046800hg38UCSC Ensembl
chr6:109366904..109368003hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216794
Samples
Known GenesSESN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604778
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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