A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3226808



Internal ID22369488
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 StatusM
Merged Variantsdgv9536n152
Supporting Variantsnssv14438577
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)nsv3226808
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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