A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14402967



Internal ID22291747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:143321778..143321778hg38UCSC Ensembl
chr8:144403948..144403948hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3553749
Supporting Variants
SamplesNA19240
Known GenesTOP1MT
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)nssv14402967
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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