A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14356455



Internal ID22283812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:881582..881656hg38UCSC Ensembl
chr11:881582..881656hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3217129
Supporting Variants
SamplesNA19239
Known GenesCHID1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14356455
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