A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14349732



Internal ID22193679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:100160955..100161394hg38UCSC Ensembl
chr9:102923237..102923676hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38440
hg19440
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3228270
Supporting Variants
SamplesHG00731
Known GenesINVS
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14349732
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