A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14267971



Internal ID22135670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:9798721..9837956hg38UCSC Ensembl
Outerchr4_gl000193_random:66035..105270hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3845938
hg1945938
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3235378
Supporting Variants
SamplesHG00513
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14267971
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