A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14259551



Internal ID22259753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:41584063..41586021hg38UCSC Ensembl
Outerchr15:41876261..41878219hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38710
hg19710
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3248071
Supporting Variants
SamplesNA19238
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14259551
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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