A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17417573



Internal ID22475443
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 StatusS
Merged Variantsnsv5905774
Supporting Variants
Samples
Known GenesFLJ34503
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17417573
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003


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