A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14262992



Internal ID22262032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:2021780..2039136hg38UCSC Ensembl
Outerchr19:2021779..2039135hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38986
hg19986
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3244980
Supporting Variants
SamplesNA19238
Known GenesMKNK2
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14262992
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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