A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908858



Internal ID22684068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:170343273..170344477hg38UCSC Ensembl
chr6:170652361..170653565hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381205
hg191205
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17415469
Samples
Known GenesFAM120B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908858
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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