A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14327675



Internal ID22136307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63418684..63419150hg38UCSC Ensembl
chr6:64128589..64129055hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38467
hg19467
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3206367
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14327675
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