A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14330486



Internal ID22116768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:159566281..159567142hg38UCSC Ensembl
chr6:159987313..159988174hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38862
hg19862
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3203214
Supporting Variants
SamplesHG00512
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14330486
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