A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3217977



Internal ID22363477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:126868431..126893075hg38UCSC Ensembl
Outerchr9:129630710..129655354hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3824645
hg1924645
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14281299
SamplesNA19238
Known GenesZBTB34
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3217977
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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