A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3241371



Internal ID22374954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:119662545..119672973hg38UCSC Ensembl
Outerchr10:121422057..121432485hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38769
hg19769
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14252825, nssv14252824
SamplesNA19238, HG00731
Known GenesBAG3
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3241371
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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