A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14278655



Internal ID22121301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:155313190..155351766hg38UCSC Ensembl
Outerchr7:155104900..155144468hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg387003
hg197003
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3217261
Supporting Variants
SamplesHG00512
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14278655
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer