A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3223830



Internal ID22367482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68964102..68964681hg38UCSC Ensembl
chr10:70723858..70724437hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38580
hg19580
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14352240
SamplesHG00732
Known GenesDDX21
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3223830
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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