A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3222021



Internal ID22366224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36778971..36785478hg38UCSC Ensembl
chr21:38151272..38157779hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg386508
hg196508
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14301979, nssv14301978
SamplesNA19238, NA19240
Known GenesHLCS
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3222021
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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