A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14271038



Internal ID22127687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:2104879..2127068hg38UCSC Ensembl
Outerchr1:2036318..2058507hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg381472
hg191472
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3214582
Supporting Variants
SamplesHG00512
Known GenesPRKCZ
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14271038
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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