A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3217938



Internal ID22363445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:157765588..157774936hg38UCSC Ensembl
Outerchr6:158186620..158195968hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg381175
hg191175
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14277656, nssv14277655
SamplesNA19238, HG00513
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3217938
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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