A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14263162



Internal ID22232111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:18688269..18733679hg38UCSC Ensembl
Outerchr19:18799079..18844489hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg383232
hg193232
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3232003
Supporting Variants
SamplesHG00733
Known GenesCRTC1
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14263162
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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