A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3238750



Internal ID22374247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:51741418..51752483hg38UCSC Ensembl
Outerchr14:52208136..52219201hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg3825777
hg1925777
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14258226
SamplesHG00732
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3238750
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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