A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14262175



Internal ID22272554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:57962475..57978247hg38UCSC Ensembl
Outerchr17:56039836..56055608hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38849
hg19849
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3236276
Supporting Variants
SamplesNA19239
Known GenesVEZF1
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14262175
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