A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17425599



Internal ID22483469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:112041851..112043442hg38UCSC Ensembl
chr6:112363054..112364645hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381592
hg191592
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5888420
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17425599
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002


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