A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14274603



Internal ID22153230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:161609934..161628053hg38UCSC Ensembl
Outerchr1:161579724..161597843hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3880483
hg1980483
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3212981
Supporting Variants
SamplesHG00514
Known GenesFCGR3B
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14274603
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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