A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16890199



Internal ID167620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9259168..9344062hg38UCSC Ensembl
chr1:9319227..9404121hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3884895
hg1984895
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5418877
Supporting Variants
Samples
Known GenesH6PD, SPSB1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16890199
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00203


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