A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16897214



Internal ID172291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:224311544..224311615hg38UCSC Ensembl
chr1:224499246..224499317hg19UCSC Ensembl
Cytoband1q42.11
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5450973
Supporting Variants
Samples
Known GenesNVL
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16897214
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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