A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3226286



Internal ID22369140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:34040043..34096634hg38UCSC Ensembl
Outerchr17:32367062..32423653hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3856592
hg1956592
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14261393
SamplesHG00732
Known GenesASIC2
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3226286
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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