A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14384900



Internal ID22298362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:46776408..46776408hg38UCSC Ensembl
chr1:47242080..47242080hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3532189
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)nssv14384900
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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