A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14299260



Internal ID22186068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:9754623..9767107hg38UCSC Ensembl
chr4_gl000193_random:21937..34421hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3812485
hg1912485
Variant TypeCNV duplication
Copy Number6
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3222074
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14299260
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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