A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14358178



Internal ID22196633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:46910691..46911864hg38UCSC Ensembl
chr11:46932242..46933415hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg381174
hg191174
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3229206
Supporting Variants
SamplesHG00731
Known GenesLRP4
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14358178
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