A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14301855



Internal ID22186850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:32342708..32342708hg38UCSC Ensembl
chr21:33715017..33715017hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3562092
Supporting Variants
SamplesHG00731
Known GenesURB1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14301855
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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