A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17534748



Internal ID21859103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:153690083..153690144hg38UCSC Ensembl
chr1:153662559..153662620hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5981459
Supporting Variants
Samples
Known GenesNPR1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17534748
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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