A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17418559



Internal ID22476429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:19730503..19730567hg38UCSC Ensembl
chr6:19730734..19730798hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5888492
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17418559
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.088


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