A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14329445



Internal ID22118476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:83237355..83237408hg38UCSC Ensembl
chr6:83947074..83947127hg19UCSC Ensembl
Cytoband6q14.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3194521
Supporting Variants
SamplesHG00512
Known GenesME1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14329445
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