A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17411023



Internal ID22468893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166147378..166151046hg38UCSC Ensembl
chr6:166560866..166564534hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg383669
hg193669
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5909571
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17411023
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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