A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14277105



Internal ID22139845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:93778457..93802259hg38UCSC Ensembl
Outerchr10:95538214..95562016hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3823803
hg1923803
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3224747
Supporting Variants
SamplesHG00513
Known GenesLGI1
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14277105
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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