A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14258532



Internal ID22192543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:25737153..25767596hg38UCSC Ensembl
Outerchr15:25982300..26012743hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38792
hg19792
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3239450
Supporting Variants
SamplesHG00731
Known GenesATP10A
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14258532
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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