A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3217068



Internal ID22362847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:216774862..216783562hg38UCSC Ensembl
Outerchr1:216948204..216956904hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38749
hg19749
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14266113, nssv14266112
SamplesNA19238, HG00513
Known GenesESRRG
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3217068
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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