A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3235029



Internal ID22373184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:81170361..81207013hg38UCSC Ensembl
Outerchr15:81462702..81499354hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38965
hg19965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14259465, nssv14259466
SamplesNA19239, HG00513
Known GenesIL16
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3235029
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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