A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905774



Internal ID22680966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:113906261..113906461hg38UCSC Ensembl
chr6:114227425..114227625hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38201
hg19201
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17417573
Samples
Known GenesFLJ34503
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5905774
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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