A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3287432



Internal ID22385835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:75383648..75383738hg38UCSC Ensembl
chr9:77998564..77998654hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9603n152
Supporting Variantsnssv14392149
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsSequences at least 70% masked by tandem repeat finder or contained within a tandem repeat
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3287432
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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