A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526807



Internal ID22396190
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14294857, nssv14294856
SamplesHG00732, HG00733
Known GenesDUSP27
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526807
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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