A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3224610



Internal ID22367987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:125738515..125740389hg38UCSC Ensembl
Outerchr9:128500794..128502668hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg381875
hg191875
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14281954
SamplesNA19239
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3224610
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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