A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14259092



Internal ID22193392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:28404963..28506689hg38UCSC Ensembl
Outerchr15:28650109..28751835hg19UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3842177
hg1942177
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3237550
Supporting Variants
SamplesHG00731
Known GenesMIR4509-1, MIR4509-2, MIR4509-3
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14259092
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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