A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3229702



Internal ID22371467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:131354457..131364596hg38UCSC Ensembl
Outerchr9:134229844..134239983hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg3810140
hg1910140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14283676
SamplesHG00732
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3229702
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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