A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14273069



Internal ID22152682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:151855278..151894725hg38UCSC Ensembl
Outerchr4:152776430..152815877hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3839448
hg1939448
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3197787
Supporting Variants
SamplesHG00514
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14273069
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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