A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14327581



Internal ID22206526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:28216651..28218550hg38UCSC Ensembl
chr6:28184429..28186328hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3199363
Supporting Variants
SamplesHG00732
Known GenesTOB2P1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14327581
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