A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14442672



Internal ID22238892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76619300..76619300hg38UCSC Ensembl
chr11:76330344..76330344hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38604
hg19604
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3556856
Supporting Variants
SamplesHG00733
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)nssv14442672
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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