A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3227885



Internal ID22370236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:138226416..138253879hg38UCSC Ensembl
chr9:141116866..141144329hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3827464
hg1927464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9862n152
Supporting Variantsnssv14391693
SamplesNA19240
Known GenesFAM157B
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3227885
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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