A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14264688



Internal ID22134620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:103117570..103143857hg38UCSC Ensembl
Outerchr2:103734028..103760315hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg3826288
hg1926288
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3206936
Supporting Variants
SamplesHG00513
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14264688
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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