A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5901854



Internal ID22677007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:116547779..116558686hg38UCSC Ensembl
chr6:116868942..116879849hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg3810908
hg1910908
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17420066
Samples
Known GenesFAM26D
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5901854
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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