A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14273062



Internal ID22265071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:149309647..149354144hg38UCSC Ensembl
Outerchr4:150230799..150275296hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg3844498
hg1944498
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3194264
Supporting Variants
SamplesNA19238
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14273062
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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