A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14384571



Internal ID22330490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:93914368..93914368hg38UCSC Ensembl
chr10:95674125..95674125hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38250
hg19250
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3555304
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)nssv14384571
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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