A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3219255



Internal ID22364333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:86042776..86116715hg38UCSC Ensembl
Outerchr9:88657691..88731630hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3873940
hg1973940
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14282905
SamplesHG00731
Known GenesGOLM1
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3219255
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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