A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14273665



Internal ID22185466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:27760221..27824998hg38UCSC Ensembl
Outerchr5:27760328..27825105hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3864778
hg1964778
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3203138
Supporting Variants
SamplesHG00731
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14273665
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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