A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3229425



Internal ID22371286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65522563..65536558hg38UCSC Ensembl
chr9:44799291..44813237hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3813996
hg1913947
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9573n152
Supporting Variantsnssv14439221
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3229425
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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