A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3198565



Internal ID22348270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13781227..13781752hg38UCSC Ensembl
chr6:13781459..13781984hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg38526
hg19526
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14327493
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3198565
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