A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14291017



Internal ID22222072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1005741..1006147hg38UCSC Ensembl
chr19:1005740..1006146hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38407
hg19407
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3210757
Supporting Variants
SamplesHG00733
Known GenesGRIN3B
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14291017
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