A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14267689



Internal ID22121618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:42585488..42592213hg38UCSC Ensembl
Outerchr21:44005598..44012323hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg382775
hg192775
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3238401
Supporting Variants
SamplesHG00512
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14267689
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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