A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3539026



Internal ID22408197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7944971..7945439hg38UCSC Ensembl
chr19:8009856..8010324hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38469
hg19469
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14285258
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3539026
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