A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14262299



Internal ID22264273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:14840003..14861134hg38UCSC Ensembl
Outerchr18:14840002..14861133hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3821132
hg1921132
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3218367
Supporting Variants
SamplesNA19238
Known GenesANKRD30B
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14262299
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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