A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14294856



Internal ID22207883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:167102932..167102995hg38UCSC Ensembl
chr1:167072169..167072232hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3526807
Supporting Variants
SamplesHG00732
Known GenesDUSP27
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14294856
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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