A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14272863



Internal ID22198027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:149621464..149658490hg38UCSC Ensembl
Outerchr4:150542616..150579642hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg3837027
hg1937027
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3195344
Supporting Variants
SamplesHG00732
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14272863
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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