A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16908019



Internal ID6133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109915041..109915084hg38UCSC Ensembl
chr1:110457663..110457706hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5550599
Supporting Variants
Samples
Known GenesCSF1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16908019
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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