A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14357192



Internal ID22239702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1684401..1697250hg38UCSC Ensembl
chr11:1705631..1718480hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3812850
hg1912850
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3229270
Supporting Variants
SamplesHG00733
Known GenesFAM99B, KRTAP5-6, MOB2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14357192
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