A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17413123



Internal ID22470993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:111645921..111646529hg38UCSC Ensembl
chr6:111967124..111967732hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38609
hg19609
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5892511
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17413123
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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