A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14438577



Internal ID22181721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:34643734..34644330hg38UCSC Ensembl
chr9:34643731..34644327hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38597
hg19597
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3226808
Supporting Variants
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14438577
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