A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14359765



Internal ID22248282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62562533..62563047hg38UCSC Ensembl
chr11:62330005..62330519hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38515
hg19515
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3530025
Supporting Variants
SamplesHG00733
Known GenesEEF1G
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14359765
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