A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14259466



Internal ID22283612
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3235029
Supporting Variants
SamplesNA19239
Known GenesIL16
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14259466
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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