A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14282915



Internal ID22207405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:24624185..24685779hg38UCSC Ensembl
Outerchr9:24624183..24685777hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3861595
hg1961595
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3215101
Supporting Variants
SamplesHG00732
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14282915
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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