A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14301257



Internal ID22135845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:6570445..6579098hg38UCSC Ensembl
chr21:44598017..44606670hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg388654
hg198654
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3227030
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14301257
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