A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14352240



Internal ID22208125
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3223830
Supporting Variants
SamplesHG00732
Known GenesDDX21
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14352240
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer