A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225789



Internal ID22368812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:42290650..42349392hg38UCSC Ensembl
Outerchr9:44621727..44676646hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3858743
hg1954920
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14282895, nssv14282894
SamplesHG00731, HG00732
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225789
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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