A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14277202



Internal ID22198785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:121821685..121840604hg38UCSC Ensembl
Outerchr6:122142831..122161750hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38794
hg19794
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3230190
Supporting Variants
SamplesHG00732
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14277202
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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