A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14281186



Internal ID22257741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:71638190..71657983hg38UCSC Ensembl
Outerchr9:74253106..74272899hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3819794
hg1919794
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3216318
Supporting Variants
SamplesNA19238
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14281186
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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