A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3244617



Internal ID22375907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:90809387..90823846hg38UCSC Ensembl
Outerchr9:93571669..93586128hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14281385
SamplesNA19239
Known GenesSYK
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3244617
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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