A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16908017



Internal ID6132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109915033..109915961hg38UCSC Ensembl
chr1:110457655..110458583hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38929
hg19929
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5414638
Supporting Variants
Samples
Known GenesCSF1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16908017
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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