A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14378282



Internal ID22328056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:95079871..95079963hg38UCSC Ensembl
chr8:96092099..96092191hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3286252
Supporting Variants
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsSequences at least 70% masked by tandem repeat finder or contained within a tandem repeat
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14378282
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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