A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14376283



Internal ID22311930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:131876016..131876016hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381031
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3544185
Supporting Variants
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14376283
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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