A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3281019



Internal ID22379337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:6977629..6977709hg38UCSC Ensembl
chr4:6979356..6979436hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14409107, nssv14455858, nssv14434750
SamplesNA19240, HG00733, HG00514
Known GenesTBC1D14
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)nsv3281019
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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