A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14282797



Internal ID22187644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:66043745..66087598hg38UCSC Ensembl
Outerchr9:42433726..42477588hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3843854
hg1943863
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3218189
Supporting Variants
SamplesHG00731
Known GenesFAM95B1
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14282797
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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