A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14387435



Internal ID22259178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:99567251..99573000hg38UCSC Ensembl
chr14:100033588..100039337hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg385750
hg195750
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3224721
Supporting Variants
SamplesNA19238
Known GenesCCDC85C
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14387435
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