A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14263684



Internal ID22120298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:50066325..50144110hg38UCSC Ensembl
Outerchr19:50569582..50647367hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3854773
hg1954773
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3233802
Supporting Variants
SamplesHG00512
Known GenesFLJ26850, SNAR-A10, SNAR-A11, SNAR-A14, SNAR-A3, SNAR-A4, SNAR-A5, SNAR-A6, SNAR-A7, SNAR-A8, SNAR-A9, SNAR-B1, SNAR-B2, SNAR-D
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14263684
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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