A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14272877



Internal ID22127747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:519604..569896hg38UCSC Ensembl
Outerchr4:513393..563685hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg385877
hg195877
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3220904
Supporting Variants
SamplesHG00512
Known GenesPIGG
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14272877
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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