A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14255591



Internal ID22200199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:115491167..115537413hg38UCSC Ensembl
Outerchr12:115928972..115975218hg19UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg3846247
hg1946247
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3219200
Supporting Variants
SamplesHG00732
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14255591
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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